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Vacant positions posted in English

Date posted Job title Location Category
16-Apr-2014 Team leader in Purchasing Service Centre (Indirect Spend)
Are you looking for new challenges? Now you have an exceptional opportunity. We are looking for a visionary and result-oriented team leader of the Purchasing team in the Purchasing Service Centre. If you know h...

Team leader in Purchasing Service Centre (Indirect Spend)

  • Finance
  • Denmark - Bagsværd

Are you looking for new challenges? Now you have an exceptional opportunity. We are looking for a visionary and result-oriented team leader of the Purchasing team in the Purchasing Service Centre. If you know how to combine long-term aspirations with needs to deliver on a daily basis you might be the ideal candidate for this position.

About the department
The Purchasing Service Centre (PSC) is responsible for the purchasing process for indirect spend in Novo Nordisk. We work closely together with our procurement colleagues in the Corporate Procurement organisation, Global Service Centre in Bangalore, our internal customers being the employees in Novo Nordisk, and the external suppliers.

The job
You will be responsible for leading and developing the purchasing and the operations in a team of 12 dedicated employees.

More specifically the team handles purchasing orders within goods and services. To successfully accomplish the task it requires good relationship to all stakeholders, may it be the procurement category managers, the customers in Line of Business, the suppliers, external auditors or various departments in Corporate Finance.

You will work closely together with the team of leaders in PSC to resolve issues and improve and develop the purchasing-to-pay process.

Qualifications
You have completed a relevant master's degree (e.g. in finance, economics or supply chain) with excellent results. You have at least 3 years of experience in line management including development and performance management of administrative employees. You have strong analytical skills and you are fluent in written and spoken English and Danish.

As a person you possess excellent communication and presentation skills and you are able to interact across functions on all levels in the organisation. You have a strong quality mind-set and you are well organized and combine your leadership skills with goal orientation and a tactical approach to problem solving. Additionally, you enjoy working in a dynamic and changing environment and you have a proactive approach to tasks and challenges.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please call Nicolai Thorborg on +45 3079 5927 or Lars Adrian Møller on +45 3079 5199.

Deadline
1 May 2014

Denmark - Bagsværd Finance
16-Apr-2014 Intern to CMC Business Support
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Intern to CMC Business Support

  • Student and Internships
  • Denmark - Bagsværd

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
The internship is in CMC Business Support, a department in CMC Supply responsible for developing and maintaining processes and systems to support the planning of a very ambitious pipeline of drug development projects in CMC Supply. One of the key elements in securing strong operations of a large project portfolio is the CMC Planning project, which is aiming at establishing a solid and transparent process allowing all drug development projects to establish and maintain overviews of the projects material demand and supply situation.

The job
You will get the opportunity to participate in implementation and updates of some of our smaller but important IT systems in CMC Supply. This requires that you familiarize yourself in the system functionality and the user requirements. You will get involved in the creation of test cases, execution of user tests and documentation of the system functionality. Furthermore your tasks will include system description in user guides and creation of training material. For the right candidate the job will also be an opportunity to influence the future integration between the IT systems and the material- project- and financial- planning process.

Qualifications
We are looking for an intern who is passionate about planning processes and systems. You are currently studying on your master’s degree in engineering, Supply Chain Management or other relevant field. Our preferred candidate is service minded, ambitious, outgoing and thriving in a busy environment. Fluency in both oral and written English and excellent interpersonal skills are required. Danish language skills are a prerequisite.

Practicalities

Qualification: Students in their first or second year of their master studies

Period: The internship position is a full-time position for 5-6 months.

Start date: Preferably 01-Sep-2014.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please contact Helle Rasmussen + 45 3075 5021 or Anne Blichfeldt Møller + 45 3079 6982.

Deadline
2 June 2014.

Denmark - Bagsværd Student and Internships
16-Apr-2014 Regulatory Affiliate Supporter
In Regulatory Affiliate Support, we are looking for a Regulatory Affiliate Supporter, as a maternity cover, to join a dedicated group of people working closely together with Novo Nordisk A/S affiliates worldwid...

Regulatory Affiliate Supporter

  • Administrative
  • Denmark - Søborg

In Regulatory Affiliate Support, we are looking for a Regulatory Affiliate Supporter, as a maternity cover, to join a dedicated group of people working closely together with Novo Nordisk A/S affiliates worldwide and Regulatory Affairs product/project groups in headquarters in Denmark.

About the department
Regulatory Affiliate Support is part of Regulatory Operations within Regulatory Affairs, which makes medicine available to patients all over the world by ensuring rapid regulatory approval in all markets. Regulatory Affairs is a fast-changing field, and the 330 employees in headquarters serve as Novo Nordisk’s advocates around the world – and make a meaningful difference to our business.

You will be part of a team consisting of 15 people situated in Søborg, Denmark providing support and services across Novo Nordisk A/S projects and products.

The job
In Regulatory Affiliate Support we are responsible for supplying Novo Nordisk A/S affiliates and product/project groups with additional registration file documentation for submissions to health authorities worldwide.

As Regulatory Affiliate Supporter, you will work as the central point of contact for Novo Nordisk A/S affiliates. Your primary task will be to support with additional documentation such as samples, certificates and statements. Furthermore, management of IT systems to ensure precise update of our product portfolio in collaboration with the Regulatory Operations Team in India will also be part of the job.

The working environment is hectic and very exciting, and no two days are alike. In your daily work you will be collaborating with many different groups of people and it is a necessity that you like and are capable of handling and switching between the many queries coming from our stakeholders.

Qualifications
You have experience from working within Regulatory Affairs or the pharma industry, as well as a relevant background such as pharmaconomist, bachelor in science, laboratory technician, nurse or similar. You are a team-player, have a positive mind-set and a good sense of humour. Flexibility, managing tight deadlines and a sense of details are your strongest assets as well as a quality mind-set. Fluency in written and spoken English is a must.

As a person you are outgoing, proactive and have a strong drive. You find it easy to be in contact with many different cultures and people in various positions, and you have a global understanding and good collaborative skills. You thrive in a busy environment and bring a can-do attitude.

Please submit your application online including motivational letter and CV in English.

In Novo Nordisk A/S it is your skills, your commitment and your ambitions which help us to improve many people’s lives. In return we offer you the opportunity to work with talented colleagues, and we offer you a wide range of opportunities for professional and personal development.

Contact
For further information, please contact Tina Lindquist at + 45 3075 9652

Deadline
4 May 2014.

Denmark - Søborg Administrative
16-Apr-2014 QA Academic for release and development of new API’s
Do you want to unfold your profound QA knowledge and your huge appetite for creating results in a pharmaceutical production environment? If so, please apply for the position as QA Academic in a job that include...

QA Academic for release and development of new API’s

  • Quality
  • Denmark - Bagsværd

Do you want to unfold your profound QA knowledge and your huge appetite for creating results in a pharmaceutical production environment? If so, please apply for the position as QA Academic in a job that includes many different clinical stages of the product development.

About the department
In Chemistry, Manufacturing & Control (CMC) API QA we assure that each and every Active Pharmaceutical Ingredient (API) activity in our development and support projects live up to the cGMP requirements. The development portfolio is expanding and thus we seeking a new colleague to help us support the growth.

We are 32 colleagues in three teams. You will join the Upstream team and have 10 dedicated colleagues. Our mission is to assure that our manufacturing processes, cell banks and intermediates from the upstream API process meet the internal and external requirements. Furthermore we’re responsible for release of API for all of Novo Nordisk’s clinical trials. The production facilities and the development laboratories are located in Bagsværd and Hillerød, and you will move between the different locations and the QA office on a day-to-day basis.

The job
You assure best-in-class quality of our new manufacturing processes and API for clinical trials. Document approval in connection with development, manufacture, stability and release of API for clinical trials as well as maintenance and improvement of the quality system (SOP’s) will constitute some of your daily tasks. In addition, you will participate in our development projects and in close cooperation with your colleagues you identify and contribute to the strengthening our stakeholders’ compliance level and act as a consultant for them.

We operate in a LEAN-dominated environment, and you will have the opportunity to contribute with ideas for improvements and drive the subsequent implementation as well. Working within QA will definitely challenge your professional and individual skills, and you will find that your tasks cover many different clinical stages of the product development.

Qualifications
You hold a Master’s degree in Pharmacy, Chemical Engineering or possess equivalent qualifications besides a strong quality mindset. You have at least 2 years’ experience with GMP, product release, production or quality assurance. As we operate both in a national and an international environment, you must speak and write Danish and English fluently.

You are ambitious and determined on creating world-class results and ensure quality of the highest order. Moreover, you thrive in a role where you use your knowledge and bring your arguments and negotiation skills into play. You are able to adapt but also challenge our way of working so that we constantly improve our methods and processes.

At Novo Nordisk, you will be part of a company respected equally for its financial results and its business ethics. Across geographical, cultural and professional communities we develop and deliver innovative medicines.

Contact
For further information, please contact Lisbeth Voetmann at +45 3075 0530 or Peter Søtofte Elten at +45 3079 8453.

Deadline
4 May 2014.

Denmark - Bagsværd Quality
16-Apr-2014 Laboratory technician
The analysis and characterization team of the Protein Chemistry department is looking for a laboratory technician. ...

Laboratory technician

  • Research & Development
  • Denmark - Måløv

The analysis and characterization team of the Protein Chemistry department is looking for a laboratory technician.

About the department
The department is part of the Diabetes Protein Engineering function of the Diabetes Research Unit, located in Måløv, north-west of Copenhagen. We are involved in early phase discovery of new therapeutic peptides and protein candidates for treatment of diabetes and obesity. The team consists of 8 scientists, 8 laboratory technicians, and one Postdoc. All our team members contribute to multidisciplinary research projects within our area of expertise that is analysis method development and mass spectrometric characterization of peptides and proteins.

The job
You will primarily work with development of HPLC/UPLC-based liquid chromatography separation methods as well as characterization of proteins and peptides using various mass spectrometric techniques. Your work will involve analysis of protein/peptide samples, development of analysis methods, data processing, and reporting of results. Your daily tasks will include planning and execution of experimental laboratory work and reporting and documentation of result in cooperation with a scientist in the team.

Qualifications
We are looking for a highly motivated laboratory technician with a solid background within HPLC/UPLC and mass spectrometric characterization of proteins and peptides. Experience with method development is an advantage, as is experience with Empower or other chromatographic software packages. Knowledge of software for evaluation of LC-MS data is a plus. You are well acquainted with general PC/IT use and have good communication skills in both Danish and English. At a personal level you possess a positive mindset and flexible attitude.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For more information on the position, please contact Niklas Gustavsson at + 45 3075 9140

Deadline
14 May 2014.

Denmark - Måløv Research & Development
16-Apr-2014 Internship in Business Support
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship in Business Support

  • Student and Internships
  • Denmark - Bagsværd

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
Strategic Sourcing is the central sourcing unit in Novo Nordisk’s Product Supply division, and we are responsible for the strategic sourcing activities related to Novo Nordisk’s worldwide pharmaceutical production sites as well as global management of suppliers. In Business Support we drive cross-unit projects and contribute to value-adding financial, commercial and market intelligence to the other three departments in Strategic Sourcing. You will enter a fast-paced and ambitious environment where we collaborate closely with stakeholders inside as well as outside Novo Nordisk. You will be located in Bagsværd, where 10 competent colleagues look forward to welcoming you.

The Job
As intern in Business Support your job will be to act as support to larger projects in the department. Furthermore, you will be supporting some of our standard reporting processes within quality and compliance. In addition it will be your responsibility to complete various analyses and manage large data sets. You can anticipate varied working days with many different tasks and numerous stakeholders. You will be considered an integrated member of the department and you will receive continuous feedback on your work.

Qualifications
You are currently studying on your master’s degree in International Business, Supply Chain Management, Economics or similar. In any case, you have sharp analytical skills and knowledge about project management. You are expected to have a flair for IT and be a super user of MS Office. To drive your projects successfully (with supervision), you need a structured approach, have a critical eye for details and a mind focused on quality. In addition, you characterise yourself as a flexible person with an unmistakably high level of drive. Good cooperation skills are essential and the ability to work in a complex and dynamic organisation is a prerequisite. Last but not least, you have solid English language skills in speech and in writing.

You are an outgoing person with a strong personal drive and dedication. You have professional and personal impact that is reflected in your desire to take initiative. In addition, you thrive in a busy environment and bring a can-do attitude and a healthy sense of humour to your work – even when the pressure is on. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

Practicalities

Qualification: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 1 September 2014

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Contact
For further information, please contact Lau Brüniche-Olsen +45 3079 0569.

Deadline
2 June 2014.

Denmark - Bagsværd Student and Internships
16-Apr-2014 Internship with focus on Quality improvement, Novo Nordisk
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship with focus on Quality improvement, Novo Nordisk

Learn more about the largest site in Novo Nordisk's global production network using this link www.novonordisk.com/kalundborg-careers

  • Student and Internships
  • Denmark - Kalundborg

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
You will join our Aspart purification Department – Aspart is Novo Nordisk’s fast acting insulin. We are part of Insulin Manufacturing 1 with a total of 390 people in Kalundborg. You will also be part of our very strong Quality team where cooperation and unity are key words. Novo Nordisk in Kalundborg is a city within the city. The area is situated a good hour from Copenhagen and covers 1,350,000 m2, including a private roadgrid. We produce some 50 % of the insulin in the world.

The job
You will be part of our quality organisation – a very important cross-functional group working together with a lot of colleagues throughout the organisation. You and the rest of the quality group are key persons to ensure that we pass important inspections from the authorities – hereby also ensure that new quality standards and requirements are implemented throughout the organisation. You are working cross-organisational to prepare new standards to ensure standardised work. Through daily sparring with production and support functions you are setting direction on quality – working closely together we obtain new quality standards.

Qualifications
We are looking for an intern who is passionate about Quality and production processes. You are currently pursuing a master’s degree in Chemistry, Biotechnology, pharmacy, public health, Engineer or other relevant field.

We expect candidates to be service minded, thrive in a busy environment and bring a can-do attitude. Ability to manage a large volume of projects and assignments (with supervision); sound personal judgment; and excellent interpersonal skills are required.

You are an outgoing person with a strong personal drive and dedication. You have professional and personal impact that is reflected in your desire to take initiative. In addition, you thrive in a busy environment and bring a can-do attitude and a healthy sense of humour to your work – even when the pressure is on. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

In combination with your natural interest in others and your ability to put yourself in charge you master the fine art of knowing when to compromise and when to stand firm. You are able to independently plan and drive your own tasks. If you do not already master Excel, you demonstrate your fast learning capabilities here as well.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Practicalities

Requirement: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 01-08-2014

Contact
For further information, please call Ane Winther Borch on + 45 3079 8487.

Deadline
2 June 2014.

Denmark - Kalundborg Student and Internships
15-Apr-2014 Internship in Global Talent Attraction, Novo Nordisk
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship in Global Talent Attraction, Novo Nordisk

  • Student and Internships
  • Denmark - Bagsværd

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
Global Talent Attraction is part Corporate People and Organisation (Corporate HR) at Novo Nordisk A/S. Our main objective is to increase the knowledge and attractiveness of Novo Nordisk as a workplace across our key markets. We function as a centre of excellence for our business areas and help them address their specific challenges in attracting and recruiting new employees. You get the opportunity to join a team of 13 employees with a variety of backgrounds (HR, communication, marketing and international business). We use our differences to create novel ideas, attraction campaigns and high-quality solutions.

The job
We have a constant focus on optimising our activities and brand towards students in Denmark as well as globally, which is one of the areas you will be involved in during the internship. You will take part in various projects and tasks related to employer branding, workshop planning, working with social media, communication materials, benchmarking analysis, etc. The right candidate will have plenty of opportunities to influence the projects he/she will be involved in.

Qualifications
We are looking for an intern who is passionate about branding and communication. You are

currently studying on your master degree in communication, marketing, HR or related fields.

The ideal candidate has some experience with branding or event management. Some

knowledge of Photoshop and/or InDesign would also be an advantage.

You are an outgoing person with a strong personal drive and dedication. You have professional and personal impact that is reflected in your desire to take initiative. In addition, you thrive in a busy environment and bring a can-do attitude and a healthy sense of humour to your work – even when the pressure is on. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

Practicalities

Requirement: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 1 September 2014

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please call Caroline E. Bloch Poulsen-Hansen on + 45 3075 2347.

Deadline
2 June 2014.

Denmark - Bagsværd Student and Internships
15-Apr-2014 Department LEAN Coordinator – production, drive and engagement
Do you have the drive to work closely with team leaders and employees on the production floor, using your LEAN mind-set and tools to improve how we deal with our daily challenges? If yes, then we have the job f...

Department LEAN Coordinator – production, drive and engagement

  • Production
  • Denmark - Hillerød

Do you have the drive to work closely with team leaders and employees on the production floor, using your LEAN mind-set and tools to improve how we deal with our daily challenges? If yes, then we have the job for you.

About the department
The department consist of 2 teams with approximately 40 employees in total. Our purpose is to ensure packaging of our Flexpen© and make sure that we deliver as promised when it comes to quality, compliance and deadline. We also deliver support to the packaging production and ensure 24/7 production time.

The job
As Department LEAN Coordinator you will report to our department manager and will be part of the department management group. You will also have dotted line to the LEAN Partner for the Vice President. Your main role will be to continuously improve LEAN competencies and support different LEAN activities — all focused on improving stability and quality across our production sites in Denmark.

You will therefore be spending most of your time on the production floor, supporting leaders in development of systems e.g. performance boards, problem solving and process confirmation. Your focus will be to see, solve and follow-up on problems, in a way that secures sustainable results. A part of your responsibility will also be to coach others to use and continuously improve the applied systems. When it comes to solving problems you will sometimes be responsible for driving the process and sometimes be supporting others in implementing and sustain defined solutions.

Besides leaders in your area you work closely together with a wide team of LEAN Partners, HR Partners and Training Partners within your assigned area. An outcome of this will be cross functional LEAN projects, defining and supporting improvement projects in your area and ensure on-boarding of new leaders in respect to the LEAN framework.

Qualifications
You hold a B.Sc., M.Sc. or similarly and through your studies and working experience you have gained a good understanding and have a great interest in being part of a process production setup. You can give examples of being part of; complex problem solving, systematic approach to problem solving, experience with applying different LEAN tools and experience that demonstrates a desire to drive change.

On a personal level, you have excellent communications skills both oral and written in Danish and English and show a natural interest in others. You are known as a fast learner with a desire to develop yourself and others and have a naturally strong personal drive and thrive driving your tasks independently. Are you talented and have the ambitions, taking up this job as Department LEAN Coordinator, might develop you into a future manager.

In Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.

Contact
For further information, please call Nicolai Banck on + 45 3079 0484 or Marianne Baatrup Thystrup on + 45 3079 6662.

Deadline
4 May 2014.

Denmark - Hillerød Production
15-Apr-2014 Internship in Biopharm Operations, Strategy & Sourcing
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship in Biopharm Operations, Strategy & Sourcing

  • Business Support
  • Denmark - Måløv

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
Novo Nordisk is seeking an engaged student for full time internship to BRU Operations in a period of 4-6 months. BRU Operations is part of Biopharmaceuticals Research Unit (BRU) which develops new research projects within three therapeutic areas; haemophilia, growth hormone and inflammation. BRU is a global organisation with 600 employees split between Måløv, Seattle and Beijing

The job
You will be working in a dynamic team with 6 other dedicated employees in Måløv. The department’s main responsibility is to deliver high quality support to management through ensuring effectiveness and efficiency in business processes, management presentations, balance scorecard process, secure portfolio planning and prioritisation as well as participation in multiple projects optimisation projects.

During your internship you will be responsible for individual deliverables and will participate in larger cross functional projects. You will be given a unique opportunity to gain a broad insight to the business and key processes. You will get hands-on project management experience in a dynamic environment, working with a dedicated and ambitious team.

Qualifications
You are currently pursuing a Master’s degree in Finance, Business Administration, Engineering or another relevant degree, and have had excellent result during your studies. You pay attention to details and possess good communication skills. You like being part of a professional team, have a high energy level, take initiative (proactive thinking) and work with a high level of engagement. You are motivated by being challenged both professionally and personally. You have a flair for IT (Excel and Power Point) and numbers. We expect candidates to be service minded, thrive in a busy environment and bring a can-do attitude. The atmosphere in BRU Operations is informal and humorous.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Practicalities

Qualification: Students in first or second year of master degree

Period: The internship position is a full-time position for 4-6 months.

Desired start date: 1 August 2014

Contact
For further information, please call Anders Mikkelsen on + 45 3079 4461.

Deadline
1 June 2014.

Denmark - Måløv Business Support
15-Apr-2014 QA Assistant
Do you want to work with Quality Assurance and secure quality mind set in a complete supply chain. Do you like cooperate with our internal stakeholders all over the world and secure timely approval of materials...

QA Assistant

  • Quality
  • Denmark - Bagsværd

Do you want to work with Quality Assurance and secure quality mind set in a complete supply chain. Do you like cooperate with our internal stakeholders all over the world and secure timely approval of materials? Then we have the right job for you in Sourcing QA.

About the department
Sourcing QA, Team Printed Packaging Materials is responsible for Quality Assurance of Printed Packaging Materials going into Novo Nordisk A/S Products. The team is responsible approval of Printed Packaging Materials for all Danish packaging sites, setting direction and approve specifications for Printed Packaging Materials worldwide. In the years to come we are facing challenges regarding global alignment between our NN production sites and standardisation of frame methods for quality control and batch releases. The team consist now of 3 QA assistants and 7 QA professionals.

The Job
You will work closely together with the 2 other QA assistants and be responsible for timely approval of Master data in SAP and MPO approval in PRISM, Review of batch documentation and disposition of printed packaging materials from our QC incoming control. Furthermore you will support the team in daily tasks such as updating relevant documents, review of NC and IC’s, data analysis and archiving GMP documentation. Challenges. We work in a dynamic and challenging environment with short deadlines, so you must be able to make prioritisations and take responsibility for customer requirements also when the solution is not obvious. You must be capable of working independently and support the team in the daily tasks. We have a high focus on launches and lead times in order to secure a high level of quality and compliance in the entire supply-chain from our suppliers to release of products.

Qualifications
Relevant technical or academic rank. You have a strong quality mind set and a good knowledge of GMP rules and quality assurance in the pharmaceutical industry. As we are cooperating broadly with many stakeholders (QC, Regulatory department, R&D) good collaboration and communication skills are needed. As a person you are known for your positive mind set and you enjoy working in a dynamic environment with many simultaneous tasks and changing priorities. You must be fluent in Danish and English, both written and spoken. We offer a very exciting job with excellent development opportunities among highly competent colleagues in a positive working environment.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please call Karin Løbel-Moberg on + 45 3075 8463.

Deadline
25 April 2014.

Denmark - Bagsværd Quality
15-Apr-2014 Training Development Consultant
Can you help Corporate Quality set the direction for future training? Do you have a proven record in developing targeted and worthwhile training that supports the business needs? Do you thrive in a busy, growin...

Training Development Consultant

  • Quality
  • Denmark - Bagsværd

Can you help Corporate Quality set the direction for future training?

Do you have a proven record in developing targeted and worthwhile training that supports the business needs?

Do you thrive in a busy, growing and global environment? ….then go for this job!

About the department
Quality Development is part of the Corporate Quality organisation in Novo Nordisk. We are a vibrant and experienced group of project managers, process experts and training development consultants all working to improve the Quality Management System. We are 26 dedicated employees organised in 3 departments: Quality Intelligence, Quality Projects and Quality Capability Development (QCD). The departments are located in Bagsværd, Denmark.

The Job
As a Training Development Consultant in QCD, your primary role is to set strategic direction and drive the development and roll-out of training tools, training metrics and training standards across Corporate Quality in close co-operation with rest of the training team.

You will support and inspire the internal trainers and subject matter experts to improve existing as well as develop new training activities by providing guidance and support regarding the pedagogical design and the selection of training methods and technologies.

You take responsibility for developing, managing and hosting extensive training programs such as our Quality Academy targeting QA professionals across Novo Nordisk and work closely with Project Managers e.g. as track lead striving to facilitate and develop world class training activities supporting the roll-out of Quality Projects globally.

Qualifications
You have an academic background such as HR, communication or science but more importantly you can demonstrate clear competencies in creating internal courses together with trainers and an ability to work both on a strategic and an operational level with relevant cross organisational stakeholders.

You are expected to have a good understanding of the full training process and can show evidence of having developed and delivered high quality training, training standards and training effectiveness measures in larger, global organisations.

Knowledge about Novo Nordisk or the challenge of organising training in a major pharmaceutical company and/or experience of project management would be an advantage.

You are an enthusiastic and committed person with the passion to drive improvements to training in quality processes from concept to implementation. You are service minded, independent and persistent.

We are determined to continually improve our work and it is therefore important that you are able to see and communicate opportunities instead of limitations and achieve results.

Contact
For additional information, please contact Mette Fjord Andersson on +45 3079 4692 or Sine Martinussen on +45 3075 9576.

Deadline
7 May 2014.

Denmark - Bagsværd Quality
14-Apr-2014 Ambitious Medical Doctors with a global mindset
Join Novo Nordisk’s Pharmaceutical Medicine Programme! We’re seeking five MDs with a desire to explore career opportunities for MDs at Novo Nordisk. We don’t treat one. We treat millions...

Ambitious Medical Doctors with a global mindset

  • MD position
  • Denmark - Søborg

Join Novo Nordisk’s Pharmaceutical Medicine Programme! We’re seeking five MDs with a desire to explore career opportunities for MDs at Novo Nordisk.

We don’t treat one. We treat millions
Are you a medical doctor looking for a challenging career path in a pharmaceutical company? Would you like to be part of highly qualified and ambitious teams in a global setting? Then this is your unique opportunity to apply for a position with three job rotations where you can use your medical and scientific knowledge in an inspiring way to create better treatments and care for our patients.

Novo Nordisk is seeking ambitious medical doctors, who are interested in getting an insight into the pharmaceutical industry and have the ambition to impact lives of millions of people with diabetes and other therapy areas covered by Novo Nordisk. Our Pharmaceutical Medicine Programme is a permanent position in Novo Nordisk where the first two years are fixed in a rotation between three key departments. This position offers you the opportunity to build a life changing career with possibilities for personal and professional development, as well as a chance to work alongside the best in the field.

“I have experienced that Novo Nordisk offers me the opportunity to work with highly qualified colleagues in an informal and engaging atmosphere” (Signe Diness Vindeløv, Global Medical Affairs)

Take your career to a new level
The Pharmaceutical Medicine Programme offers you employment on regular permanent terms, starting with a two year learning journey, where you will work with three core elements of pharmaceutical industry – drug development, drug safety and medical affairs – and thus be introduced to a variety of different assignments requiring medical and scientific expertise. We offer an inspiring and ambitious working environment with a mutually rewarding commitment, alongside the flexibility that allows you to shape your own working day.

All rotations will take place at our corporate headquarter in Denmark. However, some travelling is expected. After successful completion of the two-year programme you will be offered a regular medical position in Novo Nordisk.

“It is actually very often that I seem to forget I’m working for a company that creates revenue. My focus is always on the patients need first and thereby working for Novo Nordisk doesn’t differentiate from my previous work in the clinic” (Anne Birk Østerskov, 3rd rotation, Global Development)

MD with two-five years of research and/or clinical experience
In order to qualify for the position you must hold a university degree as a Medical Doctor. You should not have previous experience within pharmaceutical industry. You must have passed post-graduate internship, have two-five years of clinical experience and preferably documented research. You must have practical and analytical skills and be capable of working in a culture of respect, teamwork and personal responsibility.

It is expected that you contribute with your own ideas as well as build upon the ideas of others. Moreover, you should be willing to travel and work in an international arena. We expect that you are fluent in written and spoken English and have a high proficiency in IT knowledge.

”The PMP programme gives you a great opportunity to practice both your scientific and personal skills in a variety of settings. Working closely with skilled people with different backgrounds and mind-sets are very inspiring and makes you learn a lot on many different levels” (Frida Emauelsson, 1st rotation, Global development)

Meet MDs at the career website
Meet both former and current MD’s and read more about the programme at novonordisk.com/PMP. Feel free to share these job opportunities by using below functionality.

Contact
For further information, please contact Programme Responsible Anne Kaas

Deadline
4 May 2014

Denmark - Søborg Human Resources
14-Apr-2014 QA Professional
Biopharm New Haemophilia API QA is looking for a talented and ambitious QA Chemist Are you ready to assure quality and develop quality mindset in Novo Nordisk Product Supply? Then we have the job for you in Bio...

QA Professional

  • Quality
  • Denmark - Hillerød

Biopharm New Haemophilia API QA is looking for a talented and ambitious QA Chemist

Are you ready to assure quality and develop quality mindset in Novo Nordisk Product Supply? Then we have the job for you in Biopharmaceuticals Quality Assurance.

About the department
Biopharm New Haemophilia API QA is a dynamic department who are responsible for the quality assurance of our new haemophilia products. In this position you will have opportunities to learn about development and production of new products for the market and also get a solid understanding of manufacturing processes.

You will become part of a team which have a high level of self-governance. The team is responsible for the quality assurance for the cultivation and purification processes, equipment and facilities in API departments in Hillerød. The job includes QA review of several types of documents related to processes, facilities and equipment. The working relations are informal and the team value professional sparring and good humour highly.

The job
As a QA professional you will be responsible for ensuring that our products are manufactured according to our marketing authorisations. In our team we handle all kind of documentation on quality matters in the API department. This includes batch documentation, deviations, validation and changes in the production. Furthermore you will participate as an expert in relevant audits and inspections. You will continuously focus on ensuring a high compliance level in the supply chain. In a dynamic and challenging environment with short deadlines you are able to make clear prioritisations and take responsibility for customer requirements in many situations, including those where the solution is not obvious.

The position offers you a unique opportunity to leave your mark on the department, great potential for personal development while realising your goals and seeing the benefits of your work. When you start you will undergo an individual and intense training program.

Qualifications
You hold a Master’s degree or equivalent in pharmaceutical sciences, engineering or a related discipline. You have a strong quality mind-set and knowledge of GMP rules and preferable you have experience with production and/or quality assurance within the pharmaceutical industry. As we are cooperating broadly with many stakeholders, excellent collaboration and communication skills are needed.

Your language skills cover proficiency in both Danish and English. You work independently and make decisions regarding quality tasks and ensure the right balance between quality demands, authority demands and business needs. At the same time, you perform well in a team-oriented environment. As a person, you are known for a high commitment to finding constructive solutions as well as taking responsibility for your assignments.

Learn more about Novo Nordisk Product Supply and working in QA using this link www.novonordisk.com/careers/QA

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please call Ditte Kivsmose Kaldor on + 45 3075 7767 or Lars Nyholm on + 45 3075 5226.

Deadline
28 April 2014.

Denmark - Hillerød Quality
14-Apr-2014 Senior Scientist
Are you interested in the in vitro pharmacology of incretin-based therapies? Are you ready to help us find new GLP-1 analogues? ...

Senior Scientist

  • Research & Development
  • Denmark - Måløv

Are you interested in the in vitro pharmacology of incretin-based therapies? Are you ready to help us find new GLP-1 analogues?

About the department
The Receptor Pharmacology team is part of the Incretin and Islet Biology department and based in the Diabetes Research Unit. The team focuses on in vitro pharmacology and biology related to our incretin-based therapy research. Receptor Pharmacology consists of 5 scientists, 8 technicians and 6 students that have responsibility for the following: screening of new analogues, development of new assays with emphasis on incretins and GPCRs, mode of action support for discovery projects, introduction of new assay technologies and support of basic research in the biology of incretin hormones

The job
Your focus will be to deliver in vitro functional and receptor binding assay results as a part of our screening program. You will also be responsible for performing mode of action studies in recombinant and natural cell systems. You will work in project teams with scientists from other areas of diabetes research and in that role will be expected to communicate your results effectively in technical reports and oral presentations.

You will be expected to keep abreast of new developments in the fields of incretin hormones and GPCR receptor pharmacology. You will also participate in international scientific conferences and collaborations.

Qualifications
You have a PhD or similar degree/experience in the biological sciences and your professional career has had a focus on receptor pharmacology. You have extensive experience in setting up cell-based assays with a focus on GPCRs. You are familiar with state-of-the-art techniques and computational tools in the field and can contribute significantly to the team in these areas. Knowledge of incretin pharmacology is preferable but not a must. You are fluent in English and understand how to succeed in an international environment.

We offer an exciting job with lots of challenges among good colleagues in a positive working environment.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information about the job please contact Jim McGuire +45 3079 6122 or Sanne Møller Knudsen +45 3075 4555.

Deadline
30 April 2014.

Denmark - Måløv Research & Development
14-Apr-2014 Senior Project Manager for hGH
Want to work with BioPharm's broad product portfolio and help us to become fast to Market? In Biopharm Manufacturing Development, we are responsible for support to our productions, the transfer of new products ...

Senior Project Manager for hGH

  • Project Management
  • Denmark - Gentofte

Want to work with BioPharm's broad product portfolio and help us to become fast to Market? In Biopharm Manufacturing Development, we are responsible for support to our productions, the transfer of new products from R & D and ongoing optimization of our many processes.

About the department
You will be part of Biopharm Project Office within our Manufacturing Development function. Main responsibilities for the Biopharm Project Office is project management of CMC-activities on marketed products; CMC coordination of life cycle management projects; execution of process improvement projects and portfolio management of Biopharm MDev projects.

The Job
As senior project manager for the Growth Hormone project portfolio you will be responsible for driving optimization projects on our marketed products and production processes and thus help to ensure that Biopharm consistently delivers optimally and achieve its strategic objectives. You will be CMC coordinator in the Lifecycle Management core team and be responsible for product optimization within the team.

Qualifications
You currently work as a project manager or line manager and has completed your academic background as a Master in engineering, pharmacy, MSc. with several years of experience in pharmaceutical production, manufacturing development, quality and lean manufacturing. Through your work, you have gained experience with the transfer of products and ensured a good insight into the production of finished goods. You thus have an understanding of the process from the cell bank to packaged product and the applicable regulatory matters. With your optimistic and flexible approach to your challenges you are able to navigate in a changing environment and take pride in completing complex projects in organizational contexts with many different stakeholders, scarce resources and high management attention. You are able to view and analyze complex issues and illustrate possible scenarios. You are convincing in your communications and ability to find the way forward. As a facilitator, you achieve consensus in relation to the direction and approach and ensure a clear structure and plan for your work. You speak and write English.

At Novo Nordisk, we work together to prevent, treat and eventually cure diabetes. Nearly 366 million people worldwide are living with diabetes today, with two people diagnosed every ten seconds. Working here is not just a way to make a living, but a way to make a difference.

Contact
For further information, please contact Henrik Melgaard at + 45 3075 7757.

Deadline
30 April 2014.

Denmark - Gentofte Project Management
14-Apr-2014 Intern
Novo Nordisk is one of the world’s most successful pharmaceutical companies. At Novo Nordisk we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join ...

Intern

  • Student and Internships
  • Denmark - Bagsværd

Novo Nordisk is one of the world’s most successful pharmaceutical companies. At Novo Nordisk we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort.

Novo Nordisk is seeking an intern in FLIR Executive Office in Bagsværd from 11 August 2014 to support our efforts in supporting management decisions and managing our Quality function.

About the department
FLIR Executive Office consists of a management support unit and an internal consultancy - both supporting our CFO in facilitating decisions and driving key projects throughout Novo Nordisk’s global organisation.

Together with FLIR Consulting, FLIR Executive Office makes up a young, diverse department consisting of 12 dedicated employees with backgrounds from top-tier consultancies or with previous Novo Nordisk experience.

The job
As an intern in FLIR Executive Office, you will drive management support and quality management processes. Your areas of responsibility include reporting on quality improvements, assessing and implementing new internal requirements, reviewing compliance levels, and generally supporting the quality function through projects and ad-hoc tasks.

You will be working closely together with the department Quality Manager and you will be exposed to senior stakeholders. You will get hands-on experience with Novo Nordisk's quality management system, as well as best practice project management methods and tools.

Qualifications
You are a master’s degree student in Business Administration, Supply Chain Management, Engineering or similar in the first or second year of your studies. You take an interest in project work, as well as process, quality and project management.

You are among the best in your class, fluent in English and are used to working independently as well as in teams. You approach tasks in a structured way with a good sense for detail. Finally you have a positive attitude.

Your development is important to us. Training and personal development are key tools to ensure continuing development of your toolbox.

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Practicalities:

Period: The internship position is a full-time position for 5-6 months

Start date: 11 August 2014

Contact
For further questions, please call Nina Correll on + 45 3075 5009.

Deadline
10 May 2014.

Denmark - Bagsværd Student and Internships
14-Apr-2014 Team Leader
Are you interested in working in an international and challenging environment where you can use your managerial and technical skills? We are looking for a new Team Leader for our sub-department IMPACT, mynovotr...

Team Leader

  • Research & Development
  • Denmark - Søborg

Are you interested in working in an international and challenging environment where you can use your managerial and technical skills? We are looking for a new Team Leader for our sub-department IMPACT, mynovotrial.com and Web Support Team of the Clinical Systems Management department. We are part of the Global Development organisation responsible for transforming promising new drug candidates into effective treatments for patients.

About the department
The department is responsible for ensuring that the Novo Nordisk global clinical IT systems support the collection and processing of clinical data. The department’s main activities are supporting the global trial teams using the systems and ensuring that the systems are available, in compliance and constantly developed to fit the customer’s needs. The department consists mostly of support staff who work closely with multi-functional and global teams on a variety of clinical and technical projects.

Clinical Systems and Data Management support several stakeholders both within and outside Global Development and upholding high quality and timely delivery are key since we support an essential part of clinical drug development in Novo Nordisk

The job
As Team Leader you will be responsible for day to day management of our dedicated IMPACT, mynovotrial.com and Web Support team providing leadership, direction and prioritisation for the unit. You will coach, mentor and develop the team in alignment with business needs and Novo Nordisk Way

You will be project manager for Clinical Systems Management activities ensuring planning and follow-up on external consultants’ deliveries. Furthermore, you will be responsible for the support to the System Owner in the day-to-day operation of the functional support services, being the primary contact for functional support.

Qualifications
You have a good understanding of the clinical development process within the pharmaceutical industry and flair for project management and IT. You understand the regulatory requirements associated with data collected in clinical systems and can transform this to support the business.

You have min. 3 years of experience with clinical trial conduct and preferably 2 years’ experience with project or line management. In addition you possess a profound knowledge of drug development and computer systems/IT.

You also have experience with development of clinical standards and knowledge of external standards and collaboration across professional and regional borders.

As a person you are out-going, motivated, and enthusiastic and have the power to influence. You are adaptable with a flexible attitude, both regarding organisation, staff and environment. We also expect that you are honest, committed and responsible as well as an organisational talent including being efficient and systematic.

The position is based in Clinical Systems & Data Management in Søborg, Denmark. Some travelling is expected due to engagement with stakeholders around the world e.g. affiliates and vendors.

At Novo Nordisk, we use our skills, dedication and ambition to help people with diabetes. We offer the chance to be part of a truly global work place, where passion and engagement are met with opportunities for professional and personal development.

Contact
For further information, please contact Henrik Lynge at +45 3075 7318.

Deadline
24 April 2014.

Denmark - Søborg Research & Development
14-Apr-2014 Sr. Research Scientist
You now have the opportunity to play a key role in developing formulations and freeze drying processes for the next generation of biopharmaceuticals. A challenging job for an experienced scientist is available ...

Sr. Research Scientist

  • Research & Development
  • Denmark - Gentofte

You now have the opportunity to play a key role in developing formulations and freeze drying processes for the next generation of biopharmaceuticals. A challenging job for an experienced scientist is available in team Biopharm Formulation Development I, a team responsible for development of biopharmaceuticals - all the way from early development to phase III clinical trials and registration.

About the department
Biopharm Formulation Development is part of Injectable Protein Formulation in the R&D area CMC Supply. As the link between research unit and production we are responsible for developing formulations and production processes for primarily freeze dried and soluble injectables of new haemostasis and inflammation products. Due to our rapidly increasing project portfolio, we are now facing new exiting challenges. Team Biopharm Formulation Development I is located in Gentofte (Copenhagen, Denmark), and consists of 6 Technicians, 7 Scientists/Specialists and one Team Leader.

The job
We offer you a position, where you will have responsibility for development of formulations and freeze drying processes assuring optimal biopharmaceutical characteristics. The development projects will be within haemophilia products, monoclonal antibodies and growth hormones. Your daily work will be in close collaboration with a project team and you will design, interpret and report studies on drug product and freeze drying processes - hereby generating pharmaceutical documentation for internal and external use. You will interact with a wide variety of internal stakeholders, e.g. Production (Product Supply), Regulatory affairs, Quality Assurance, Analytical Development, Production Pilot Plant and Discovery.

Qualifications
You hold a Master of Science possibly combined with a PhD in Chemical Engineering, Pharmacy or another relevant scientific discipline. You have working experience within drug product development. Candidates with knowledge and experience with freeze drying processes of therapeutic proteins will be preferred. As a person you are result-oriented and flexible. You enjoy working in a team with highly motivated people, dedicated to developing the next generation of biopharmaceuticals. You work systematically, have good collaborative skills and have knowledge of strict documentation standards. You possess drive and a positive mindset, and you strive to make the best scientific solutions.

At Novo Nordisk we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous scientific challenges.

Contact
For further information, please call Charlotte Rossmeisl on + 45 3075 4035.

Deadline
28 April 2014.

Denmark - Gentofte Research & Development
14-Apr-2014 Regulatory Associate
Join a fast-changing environment where engaged people do their best every day to get Novo Nordisk’s medicines approved across the globe. Our people have a unique combination of scientific insight and the abilit...

Regulatory Associate

  • Regulatory Affairs
  • Denmark - Søborg

Join a fast-changing environment where engaged people do their best every day to get Novo Nordisk’s medicines approved across the globe. Our people have a unique combination of scientific insight and the ability to navigate many agendas and stakeholders. That makes Regulatory Affairs a truly interesting place to work – but also quite challenging. Are you up for the challenge?

We are currently looking for a Regulatory Associate with an interest in working with Life Cycle Management (LCM) activities to join our Modern & Human Insulins’ team. The vacant temporary position is of 12 months duration.

About the department
The Modern & Human Insulins’ team is a part of the Regulatory Insulins and Oral proteins department. In the team, we are 10 regulatory associates and professionals working with all the clinical regulatory LCM activities for our marketed modern and human insulin products.

The job
You will be substituting one of our regulatory associates, and your primary task will be to handle the administrative tasks needed for clinical LCM of one of our modern insulin products in close collaboration with the product responsible regulatory professional, internal stakeholders and affiliates worldwide. You will be administrative responsible for preparing, compiling and submitting documentation to health authorities, and assisting in ensuring approvals. You will also be handling requests from affiliates and other stakeholders. You will work in a fast paced environment with tight deadlines, and you will be supported by a team of friendly colleagues with a good sense of humour.

Qualifications
Preferably, you have experience from working in Regulatory Affairs. You have an educational background as pharmaeconomist, medical secretary, bachelor in science, marketing, English or similar. You have a flair for IT systems and experience with MS Office applications as you will be responsible for managing data entry and electronic filing in our various databases and document management systems. Fluency in written and spoken English is a must.

On a personal level, you are very structured, systematic and you have a strong quality mind-set. You are a team player, but also enjoy working independently. You have a positive attitude, good sense of humour, and you keep your spirits high also under pressure.

At Novo Nordisk we strive for excellence. As a world leader in in deabetes care and a major player in haemostasis and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please call Dorte Tingskov on + 45 3075 8086.

Deadline
28 April 2014.

Denmark - Søborg Regulatory Affairs
14-Apr-2014 Quality Coordinator in Supply Chain Planning
Are you passionate about maintaining and improving quality and compliance? Are your keen on working internationally and have an interest in Supply Chain Management? Then, we may have the right position for you....

Quality Coordinator in Supply Chain Planning

  • Supply Chain and Logistics
  • Denmark - Bagsværd

Are you passionate about maintaining and improving quality and compliance? Are your keen on working internationally and have an interest in Supply Chain Management? Then, we may have the right position for you. As Quality Coordinator, in Shipping and Customer Service, a department within Supply Chain Planning, you will play a key role in ensuring that the department constantly meets the regulatory requirements within ISO and GMP. You will become part of a dynamic work environment with direct access to our global customers.

About the department
You will be a part of the Shipping & Customer Service department, which handles shipping of finished products and raw materials. 37 dedicated colleagues ensure fast and reliable global import/export of Novo Nordisk’s products to our affiliates and direct customers around the world in the right quality and at competitive prices.

The job
As Quality Coordinator, you are quality responsible for the department and support and guide the unit in quality related issues. This includes acting as unit GxP training coordinator as well as unit review coordinator and handling the change requests and

non-conformities relating to transport.

Additionally, you are responsible for transport process validation, e.g. ensuring quality and compliance when transporting Novo Nordisk’s products. In particular, it is your responsibility to make protocols and document that the products stay within the specific standards of tolerance from the moment they leave the ramp at Novo Nordisk until they reach the final destination somewhere in the world. You play a key role in preparing and presenting validation documents for Danish and international authorities, and you participate in the audits and inspections, giving a detailed account of the validation methods and the results.

Furthermore, you will contribute to managing the daily use and maintenance of the IT system used for temperature monitoring during transport and for validation in connection with upgrade and changes to the system.

You can look forward to a global and independent job, where you will be in contact with stakeholders from all over the world and play a major role in our efforts to live up to all QA and QC requests.

Qualifications
You have a Msc in Engineering, Pharmacy or similar, combined with experience from a similar position or a position within QA or QC. It is an advantage if you also have experience with process validation. In everything you do, you are driven by your strong personal commitment and sense of responsibility and you are not afraid to stand your ground when needed. You have a systematic and thorough approach to your work and you are keen on finding sustainable solutions. You have a sense of initiative and enjoy an independent role where you work as the go-to-person who possesses solid in-depth expertise within your field of work. This job also requires excellent communication and cooperation skills, as you navigate your way around colleagues, foreign authorities and other stakeholders, and balance support and continuous follow-up. Finally, you take pride in meeting your deadlines and you never compromise on quality in your work.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please call Christina Grauballe on + 45 3075 2053.

Deadline
30 April 2014.

Denmark - Bagsværd Supply Chain and Logistics
12-Apr-2014 Finance intern
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Finance intern

  • Student and Internships
  • Denmark - Hillerød

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
You will be part of a small dynamic team developing and driving Financial Management in DMS, who has global responsibility of delivering plastic components for Novo Nordisk injection pens. We value professionalism and responsibility, and have an open and informal team culture. We ensure an environment, where we focus on continuously improving individual and team competences. You will interact in teamwork with your colleagues, and have a broad list of contacts throughout the organization.

The job
You will be involved in a broad variety of activities related to Management Accounting, fx. Month end closure and Management reporting and Controlling. You will assist the team in performing follow-up on Financial Performance through daily and weekly deliverables to internal and external stakeholders on Operating Cost and Investments. Furthermore, you will solve day to day Accounting issues. As an Intern, you will get insights on how to operate a Finance function in an efficient and value adding way.

Qualifications
You want to use your solid financial knowledge and get energy from delivering results and continuously improving existing processes. You are currently studying on your master’s degree in Finance or Economics (Cand.Merc, Cand. Polit or similar). You have a solid understanding of Management Accounting and Reporting. You like working with numbers, have excellent analytical skills and you are an Excel super-user. You have fluency in both oral and written English, sound personal judgment and excellent interpersonal skills. You work in a structured way and have a sharp eye for details. You can handle many tasks simultaneously, have a strong focus on quality and wants to deliver results. As a person you are ambitious, dedicated, and you can easily interact with employees at all levels in the organization.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Practicalities

Qualification: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 1 August 2014

Contact
For further information, please contact Anders Hvidt on +45 3075 4023.

Deadline
2 June 2014.

Denmark - Hillerød Student and Internships
12-Apr-2014 Internship in Sourcing Operations Business Support, Novo Nordisk
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship in Sourcing Operations Business Support, Novo Nordisk

  • Student and Internships
  • Denmark - Bagsværd

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
You will join an exciting and ambitious supply chain organization in Bagsværd. We are responsible for the inbound supply of materials to NNs production sites world-wide. We source materials, store them, perform quality control and supply them to the production sites. We strive for running an increasingly integrated and seamless supply chain, which is what we need the right intern to support us in.

The job
You will play a key role in mapping and optimizing the flows and value stream across Sourcing Operations. You will support our Project Managers in performing Value Stream Mapping across our value chain and within specific processes. Furthermore you will based on your specific interests and competencies – be involved in concrete LEAN improvement initiatives. Your job will be a combination of teamwork and individual contributions, and you will on a daily basis interact with many different kinds of people. If you are eager to learn, engaged and takes responsibility you will experience a trusting support to your development.

Qualifications
We imagine that your master studies is somehow related to supply chain. Whether with a technical, business or natural science angle is of less importance. We expect that you are able to rapidly navigate in a complex and somewhat ambiguous environment, and thus preferably have experience with working in a larger organization. You have knowledge of and preferable experience with LEAN tools and practices. Personally you are motivated by making a difference to other people, and prefer to act in order to learn. You are fluent in building relationships and interact confidence inspiring with other people. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

Our business language is English, however in order to be able to work effectively on the shop floor, you need to have strong oral Danish skills as well.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Practicalities

Requirement: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 25-08-2014

Contact
For further information, please contact Mads Yding Lind on +45 3079 8103

Deadline
02 June 2014.

Denmark - Bagsværd Student and Internships
12-Apr-2014 Internship with focus on LEAN improvement, Novo Nordisk
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship with focus on LEAN improvement, Novo Nordisk

Learn more about the largest site in Novo Nordisk's global production network using this link www.novonordisk.com/kalundborg-careers

  • Student and Internships
  • Denmark - Kalundborg

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
You will join our new Multiline Purification Department. We are part of Insulin Manufacturing 1 with a total of 390 people in Kalundborg. You will also be part of our very strong LEAN team where cooperation and unity are key words. Novo Nordisk in Kalundborg is a city within the city. The area is situated a good hour from Copenhagen and covers 1,350,000 m2, including a private roadgrid. We produce some 50 % of the insulin in the world and w you are pursuing a master’s degree e are at the front edge of the development within technology, systems, methods and processes.

The job
Your focus is to continuously improve LEAN competencies and to support activities in order to improve stability and quality from fermentation/recovery to purification. Everybody – Managers as employees – must be equipped with the right tools that enable them to work with a very high quality mindset and as efficiently and as cost-consciously as possible. You will therefore spend a lot of your time in the production area where you spot processes and methods with LEAN improvement potential – data crunching is another part of this. You see, you solve, you share and follow-up on problems. As part of the job you support managers across the entire facility in the development of LEAN systems and methods, e.g. performance boards, problem solving and process confirmation. Standardisation, alignment and best practice sharing will be the key to your success.

Qualifications
We are looking for an intern who is passionate about LEAN, production processes and uptimization. You are currently pursuing a master’s degree in pharmacy, public health, health services research, health economics/economics or other relevant field.

We expect candidates to be service minded, thrive in a busy environment and bring a can-do attitude. Ability to manage a large volume of projects (with supervision); sound personal judgment; and excellent interpersonal skills are required.

You are an outgoing person with a strong personal drive and dedication. You have professional and personal impact that is reflected in your desire to take initiative. In addition, you thrive in a busy environment and bring a can-do attitude and a healthy sense of humour to your work – even when the pressure is on. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

In combination with your natural interest in others and your ability to put yourself in charge you master the fine art of knowing when to compromise and when to stand firm. You are able to independently plan and drive your own tasks. If you do not already master Excel, you demonstrate your fast learning capabilities here as well.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Practicalities

Requirement: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 01-08-2014

Contact
For further information, please contact Ronnie Hansen +45 3079 2995

Deadline
02 June 2014.

Denmark - Kalundborg Student and Internships
12-Apr-2014 Internship
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship

  • Student and Internships
  • Denmark - Bagsværd

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring energy and new ways of thinking to our company.

About the department
Site Denmark Data Management is seeking an engaged student for a salaried full-time internship for a period of 6 months commencing June 2014. Site Denmark (SDK) is the Danish site in Diabetes Finished Products where insulin is filled, assembled and packed within Novo Nordisk. SDK is the largest producer of finished insulin products in Novo Nordisk.

The SDK Data Management team is a newly created team dedicated to support the performance management of Site Denmark, and this particular internship takes place in Bagsværd.

The job
You will be working in young and dynamic team with four dedicated employees. Among other things we are responsible for driving the performance management across Site Denmark. During your internship you will be responsible for improving the data and visual structure of our KPIs as well as driving problem solving in ad-hoc projects. Furthermore you will be responsible for an improvement project to be defined in collaboration with your manager, which can link to your study programme.

Qualifications
You like working with numbers, have excellent analytical skills, you are an Excel super-user and have experience in programming. You are studying for a degree in Business, Engineering, Supply Chain Management or any other relevant degree. Only candidates who have not yet finalized their degree will be considered for the internship.

As a person you are ambitious, dedicated and a team-player. You have good communication skills and can easily interact with employees at all levels in the organization. Your tasks will require independence, a flexible approach and good oral and written communication skills.

You have solid interest in Data Analysis and but also curious about Supply Chain, and you can see yourself working in Novo Nordisk in the long run.

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Contact
For further information, please contact Stephane Chong on +45 3075 1072.

Deadline
2 June 2014.

Denmark - Bagsværd Student and Internships
12-Apr-2014 Internship in Process Support
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship in Process Support

  • Production
  • Denmark - Hillerød

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
You will be a part of a dynamic and high performing Process Support team in Hillerød, responsible for supporting the production of plastic components for Novo Nordisk medical devices. We value professionalism and responsibility, and have an open and informal team culture. We ensure an environment, where we focus on continuously improving individual and team competences. You will interact in teamwork with colleagues, and have a broad list of contacts throughout the organization.

The job
You will be involved in a broad variety of activities related to Process Support in day-to-day business processes and tasks.

You will assist the team in performing follow-up on Process Support performance through daily and weekly deliverables to internal and external stakeholders. As Intern, you will get insights on how to operate in Process Support in an efficient and value adding way.

Qualifications
We are looking for an Intern who is passionate about delivering results and continuously improving existing processes.

You are currently studying on your master’s degree in engineering or Cand.Merc or similar. Fluency in both oral and written English; ability to manage a large volume of projects (with supervision); sound personal judgment; and excellent interpersonal skills are required.

You are an outgoing person with a strong personal drive and dedication. You have professional and personal impact that is reflected in your desire to take initiative. In addition, you thrive in a busy environment and bring a can-do attitude and a healthy sense of humour to your work – even when the pressure is on. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

Practicalities

Qualification: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 01-08-2014

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Contact
For further information, please contact Thomas Iversen on +45 3075 6219.

Deadline
2 June 2014.

Denmark - Hillerød Production
12-Apr-2014 Intern with ambition and focus on production planning
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Intern with ambition and focus on production planning

  • Student and Internships
  • Denmark - Hillerød

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring energy and new ways of thinking to our company.

About the department
Product Supply in Novo Nordisk is seeking an engaged student for a salaried full-time internship in Site Denmark Logistics in a period of 6 months commencing August 2013. Product Supply is an organization with close to 10,000 employees located in Denmark or at one of our five international production sites. Product Supply is responsible for all production in Novo Nordisk and delivery of products to our sales affiliates or directly to major customers. Site Denmark is one of these five productions sites located in Kalundborg, Bagsværd and Hillerød, and this particular internship takes place in Hillerød.

The job
You will be working in a challenging and highly dynamic logistics team with ten dedicated employees. Among other things we are responsible for planning a production running 24/7, which requires a combination of excellent planning and fast containment of problems. During your internship you will be responsible for a number of operational tasks within FlexPen® assembly and pack including production planning in close collaboration with the production, handling raw materials & packaging materials, updating logistic KPI’s and driving problem solving. Furthermore you will be responsible for an improvement project to be defined in collaboration with your manager, which can link to your study programme.

Qualifications
You are studying for a degree in Production Engineering, Logistics, Supply Chain management or any other relevant degree. Only candidates who have not yet finalized their degree will be considered for the internship.

Besides this, personality is the key word. You are positive, independent, energetic and flexible. You see solutions instead of problems and you take initiative to implement these solutions. You get the job done.

You have solid interest in Production and Logistics, and you can see yourself working in Novo Nordisk in the long run.

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Contact
For further information, please call Carl Johan af Rosenborg on + 45 3075 6719.

Deadline
2 June 2014.

Denmark - Hillerød Student and Internships
11-Apr-2014 Director
Are you on the lookout for the opportunity to combine your scientific understanding, regulatory insight, and leadership skills? ...

Director

  • Management
  • Denmark - Søborg

Are you on the lookout for the opportunity to combine your scientific understanding, regulatory insight, and leadership skills?

About the department
At Novo Nordisk Regulatory Affairs (RA), we strive to make new and better medicines available worldwide, for among others people with diabetes and haemophilia. In the haemophilia area we currently have 2 new haemophilia drugs in phase 3 development and 1 drug under review by the regulatory authorities.

The job
As Department Director your primary focus is to manage the growing Factor VIII and Factor IX projects department which has one drug under review and two which will soon be submitted for regulatory approval. Our organisation is dynamic, with change management being an integral part of our everyday life. The job puts high demands on your leadership skills in terms of performance management and your ability to develop a staff of 15+ direct reports on the basis of individual and business needs.

You secure the quality of the documentation submitted to health authorities, and in this respect will be supported by Regulatory Project Managers, professionals, and associates in our organisation.

You report to the Corporate Vice President, RA Haemophilia and are a member of the Area’s line management team that is responsible for organisational and staff matters, including the optimising of resources across the Area. You will also be member of the wider Project management team together with our US based colleagues driving the regulatory progress of our portfolio in the US. In addition, you will be involved in cross functional projects and improvement initiatives within and outside the RA organisation, as well as collaboration with medical/clinical, marketing, product supply and quality assurance departments.

Qualifications
We expect you to have a university degree in science and a proven record of extensive global regulatory understanding and experience, successful liaison with regulatory authorities, profound understanding of haemophilia or other rare diseases, as well as cross-organisational experience in global drug development.

You have documented leadership experience: you set direction, lead and motivate your staff to work for joint objectives.

As a person you are well organised and have solid problem-solving capabilities, just as you show a winning attitude and never lose your strategic focus. You can keep your spirits high even when under pressure, and as a skilled communicator you can cooperate at any organisational level. Finally, you are comfortable using your fluent written and spoken English on a daily basis.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please contact Henrik K. Nielsen on + 45 3079 6298 or Lene G. Sommer on + 45 3075 9762

Deadline
28 April 2014.

Denmark - Søborg Management
11-Apr-2014 Talented Innovation engineer with potential to grow
Talented innovation engineer with potential to grow! Kick-start your career in one of the world’s leading companies within medical devices - located in the greater copenhagen area. Join Device Research & D...

Talented Innovation engineer with potential to grow

  • Research & Development
  • Denmark - Hillerød

Talented innovation engineer with potential to grow! Kick-start your career in one of the world’s leading companies within medical devices - located in the greater copenhagen area.

Join Device Research & Development at Novo Nordisk A/S and get a life-changing career!

Novo Nordisk A/S, a global healthcare company with 90 years of innovation and leadership in diabetes care, is looking for a newly graduated innovation engineer to take up a position in early innovation R&D.

About the department
Device Research & Development is an area within Global R&D, responsible for the development of medical devices for self-treatment within all business areas of Novo Nordisk A/S. Device Research & Development has a long and outstanding track-record of developing the best, most innovative and widely-used injection devices in the world. You will join an early innovation team of 6 highly skilled engineers and designers, responsible for the development of a next generation prefilled device.

We are located at a state-of-the-art R&D facility in the greater Copenhagen area.

To learn more about Device Research & Development, please visit: www.novonordisk.com/device-rd

The job
You will be working in the early phases of innovation including tasks related to user insights, ideation, prototyping and test. You will especially focus on transforming user needs into tangible designs suitable for mass production.

You will be given a number of different responsibilities and experience a variety of tasks, working with both internal and external stakeholders. The job will enhance your professional and personal development, providing you with an opportunity to develop skills within specialist expertise and project management.

Qualifications
You hold an academic degree (or graduate within the next 6 months) in Mechanical Engineering or similar relevant background.

You are independent, flexible and result-oriented with a ‘can-do’ attitude. You have a solid academic background and must be able to learn fast, excel at cross-functional collaboration and communicate at all levels. You must be prepared to invest significant personal effort in your work and proactively take ownership of your areas of responsibility. Finally, the strongest candidates will be those with a talent for generating attractive overall design solutions to a sometimes confusing pool of wishes and needs from users and internal stakeholders.

Proficiency in oral and written English is essential.

Device R&D is an organisation with many international employees and we welcome non-local applicants. We have great experience helping people move to Denmark and will support relocation.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please contact Steffen Hansen on + 45 3075 8423.

Deadline
24 April 2014.

Denmark - Hillerød Research & Development
11-Apr-2014 Research Scientist
We are helping increase the quality of life for people with haemophilia by doing state of the art in vivo pharmacology research. Our primary goal is to predict which drug candidates are most likely to be effect...

Research Scientist

  • Research & Development
  • Denmark - Måløv

We are helping increase the quality of life for people with haemophilia by doing state of the art in vivo pharmacology research. Our primary goal is to predict which drug candidates are most likely to be effective and of benefit to patients with haemophilia using animal models. Are you ready to use your in vivo research skills, personal drive and engagement to help us realise this goal?

About the department
We use a variety of animal models to support the Novo Nordisk haemophilia portfolio as well as the global haemophilia society in general with innovative pharmacology and advanced knowledge on the pathophysiology of haemophilia.

The department comprises four scientists with backgrounds in biology, human biology, pharmacy and veterinary medicine, six in vivo laboratory technicians, an in vivo laboratory technician trainee, and a PhD-student.

The Job
We offer an exciting and challenging job with good professional as well as personal development opportunities. You will find yourself in an inspiring and engaging environment working with highly qualified and motivated scientists in multidisciplinary teams.

Your base will be the department, but much of your work will be conducted in cross-organisational project teams with colleagues from across the biopharmaceuticals research unit. Your primary responsibilities will be to generate high quality in vivo effect data by planning, conducting and reporting proof-of-concept, dose response, and duration of effect studies. Data will be used to select and characterize the in vivo effect of the most promising drug candidates for clinical development.

Additionally, you will support marketed compounds with effect data, explore new indications or mechanisms of action and thereby help to generate ideas for novel treatments. Finally, the generation of new in vivo models for advanced haemostasis research is an important and prioritized aspect of the job.

Qualifications
You hold a PhD and a good pathophysiological understanding and experience with in vivo pharmacology. As a person you are curious, innovative, and dynamic with a positive attitude to new ideas and people; you use your excellent communication skills in everything you do. International research experience and experience with coagulation or fibrinolysis will be considered an advantage.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth

Contact
For further information, please contact Tom Knudsen on + 45 3075 1869.

Deadline
24 April 2014.

Denmark - Måløv Research & Development
11-Apr-2014 Regulatory Associate
Are you the new Regulatory Associate for Victoza? If so, you may be the associate we are looking for. ...

Regulatory Associate

  • Administrative
  • Denmark - Søborg

Are you the new Regulatory Associate for Victoza? If so, you may be the associate we are looking for.

About the department
We are a department of 11 people working with marketed Victoza that is one of our block-buster products that is used for treatment of people with type 2 diabetes. We are looking for a Regulatory Associate to join our team working mainly with the centralised procedure in the EU and with national product licenses worldwide.

The job
In close collaboration with a team of other associates, experienced professionals, and regulatory project managers you will be responsible for our administrative processes in an environment with a high pace, many different tasks and short deadlines.

You will administer and coordinate a wide range of regulatory tasks to ensure a smooth workflow in our department – but also among our stakeholders within Novo Nordisk headquarters and affiliates. Your focus will be working with clinical documents in relation to variations, renewals and new registrations. In collaboration with the team you will ensure planning as well as timely submissions of high quality applications to Health Authorities worldwide. You will ensure adherence to important internal working processes such as workflow for variation submissions world-wide as well as adherence to the many complex processes with EU centralised procedure submissions such as grouping and work-sharing.

Qualifications
You have a relevant background as a pharmaconomist, medical secretary, librarian, bachelor in science, or similar from the pharmaceutical industry. Using IT such as electronic document management systems and the Microsoft Office package professionally comes naturally to you. You are a team-player, have a positive mind-set and a good sense of humour. Flexibility, managing tight deadlines and a sense of details are your strongest assets as well as a strong quality mind-set. Fluency in written and spoken English is a must.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please contact Director Lene Melchiorsen at + 45 3079 1993.

Deadline
2 May 2014.

Denmark - Søborg Administrative
11-Apr-2014 CCGloW Expert
This is a highly versatile job where you will gain broad exposure to the company through interaction with stakeholders in R&D, Global Development and Product Supply along with our affiliates around the glob...

CCGloW Expert

  • Quality
  • Denmark - Bagsværd

This is a highly versatile job where you will gain broad exposure to the company through interaction with stakeholders in R&D, Global Development and Product Supply along with our affiliates around the globe. It requires deep process understanding, database super-user skills and excellent communication.

About the department
CCC is responsible for handling and evaluating product complaints from around the world. We work at the interface of our products and patients, and are responsible for maximizing the value of patient feedback by capturing and incorporating it back into Novo Nordisk processes. We are a part of Global Safety, located in the House of Quality in Bagsværd.

The job
The job is a permanent position and starts asap - latest 1st of July 2014.

Your main tasks are to ensure development of system improvements, and to provide tools for reporting (views) via high level SQL development tasks. This includes idea collection, specification, prioritization, testing and implementation.

You are also the bridge between users and various internal & external IT organizations. This requires excellent communication skills including the ability to translate the specialized processes & language of complaint handlers into the technical language of IT supporters & developers.

Together with colleagues, you will also be responsible for providing functional support to our 600+ users worldwide - primarily through our superuser network. This involves direct user training, coordination of our annual conference and process development.

Our users comprise production sites, R&D, and several of our international affiliates, hence in addition to bridging with IT units, you will also work broadly within Novo Nordisk.

Qualifications
You hold an academic degree in IT, engineering, mathematics, pharmaceutical sciences, or a related natural science discipline. The ideal candidate also has experience working with complaints in a production environment and programming in high level SQL.

You grasp complex processes, quickly gaining an overview while maintaining attention to detail. You communicate well – in spoken and written English - with non-technical users and IT technicians alike. In general, you are IT savvy, and work in a structured manner with a high quality mindset. You are a completer, but also flexible to changing priorities, You are a positive and open minded team player.

We offer a very exciting job amongst good colleagues with diverse backgrounds in a positive, dynamic working environment.

At Novo Nordisk, decisions and actions are based on their impact on society, the environment and on their potential to generate a profit. That makes for a responsible culture with a healthy and engaging working environment.

Contact
For further information, please call Julie Gillin on + 45 3075 6065.

Deadline
2 May 2014.

Denmark - Bagsværd Quality
10-Apr-2014 QA specialist
Are you ready to ensure compliance and high quality in the supply chain of Novo Nordisk products produced worldwide? Do you want to cooperate with stakeholders all over the world? Then we may have just the righ...

QA specialist

  • Quality
  • Denmark - Bagsværd

Are you ready to ensure compliance and high quality in the supply chain of Novo Nordisk products produced worldwide? Do you want to cooperate with stakeholders all over the world? Then we may have just the right job for you in Supply Chain Planning QA.

About the department
Supply Chain Planning QA (SCP QA) is a newly established as an independent department located in Bagsvaerd, Denmark. SCP QA is responsible for Quality Assurance and support of Supply Chain Planning activities including cold chain distribution of Novo Nordisk products produced worldwide. The department has 5 employees and is expected to grow in the coming years.

SCP QA is part of CLM & SCP QA, which is a unit in Devices & Supply Chain QA in Product Supply Quality, Novo Nordisk A/S. In our daily work we work closely together with Supply Chain Planning (SCP), which is a unit in Devices & Supply in Product Supply, Novo Nordisk A/S

Focus on Good Distribution Practice (GDP) and cold chain transportation is growing from the regulatory authorities and securing implementation and fulfilment of these requirements into Novo Nordisk’s Supply Chain is an important role of SCP QA, and makes the daily work in the department filled with new exciting challenges where not two days are similar.

The job
You will be responsible for quality assurance of Novo Nordisk supply chain processes with focus on cold chain distribution of our finished products worldwide. Implementation of GDP requirements at Novo Nordisk as well as at external partners (transport companies and warehouses) will together with quality agreements and audit support to the external partners be your main responsibility.

Beside this you and your collages in SCP QA are responsible for ensuring compliance, product quality and patient safety in SCP QA’s daily operations, and have to offer QA support and GMP guidance internally to Supply Chain Planning and affiliates and to our external partners. Your tasks will be to review and approve quality related documents such as SOP’s, deviations, transport deviations and change control cases, and you will also participate in relevant audits and inspections internally and externally.

In connection with projects like setting up a new shipping hub for all our products you will participate in the projects and must work on building close collaborations and relations with the internal and external partners involved to facilitate both the daily work and when challenging issues arise.

You will have numerous encounters daily with both internal and external business partners and you should expect a high level of complexity in your daily tasks. You will solve a wide variety of tasks and have great opportunity to be challenged every day.

As SCP QA is responsible for distribution of products world-wide, you will be working with people from different cultures and facilitate cross-cultural solutions, taking the local conditions into consideration.

Qualifications
You hold a M.Sc. in pharmacy, engineering or have an equivalent educational background and have at least 5 years of work experience related to quality assurance in pharmaceutical production, preferably within supply chain and distribution of medicinal products. You are skilled within interpretation and application of quality demands, and audit experience.

As a person, you take responsibility for your assignments, and you are solution oriented and exhibit a pragmatic attitude when solving complex issues leading you to find constructive solutions. You can take leadership in projects, and secure implementation of agreed solutions.

Quality Mindset is an integrated part of your personality and you are able to balance compliance and product quality when making decisions and can stay firm when needed to secure the quality and compliance aspects.

You will work in an international organisation with many internal and external stakeholders your ability to communicate clear and collaborate is highly required, you will need to be fluent in English both in speaking and writing.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same with a lot of interaction with stakeholders in a global business environment.

Contact
For further information, please contact Susanne Boe-Hansen on+ 45 3075 8363.

Deadline
20 April 2014.

Denmark - Bagsværd Quality
10-Apr-2014 Senior Strategy Manager
Are you looking for job where you will have an impact on the strategic- and operational development of an organisation with more than 600 employees? Are you motivated by the opportunity to be part of a winning ...

Senior Strategy Manager

  • Project Management
  • Denmark - Måløv

Are you looking for job where you will have an impact on the strategic- and operational development of an organisation with more than 600 employees? Are you motivated by the opportunity to be part of a winning team with ambitions to set new standards in a research organisation? If you have what it takes: drive, an interest for business in a science environment and a sharp mind, you may be the person we are looking for.

About the department
The Biopharmaceuticals Research Unit (BRU) is a global organisation with employees split between Måløv, Seattle and Beijing. BRU develops new research projects within three therapeutic areas; haemophilia, growth disorders and autoimmune diseases. You will be a part of the BRU Operations team in Måløv which consists of 6 dedicated employees who are ambitious and constantly strive for excellence. The department has a strong link to senior management and is driving the development of business plans, securing portfolio planning and ensuring effective and efficient business processes. Additionally, BRU Operations is running a number of cross-functional projects with participants from various functional areas.

The job
You will personally be responsible for driving one or more of our projects, and thereby the management of a steering committee and potentially a working group of 4-6 members. The job offers frequent senior management interactions and most projects have international reach. Projects include strategy, mid- and long-term planning, organisational development and process optimisation. The job holder will be involved in several ad hoc assignments such as data analysis, excel modelling and management presentations. You will be exposed to different parts of the organisation in Denmark and globally. You will build a strong network within the organisation and be able to further develop your skills. We expect you to actively take part in the continuous development of the department and contribute to a high performing team.

Qualifications
The person we are looking for has completed a relevant Master's Degree (business administration, economics or a degree within life science) with excellent results. Ideally you have 2-5 years of experience with project management, e.g. from a well-reputed consultancy or within the pharmaceutical industry. You are motivated by driving change and improvements involving many stakeholders at all levels in the organisation. You have a high level of drive, initiative and persistence and you are result-oriented. Furthermore, you are ambitious and like to be challenged. You are analytical, structured and comfortable managing a project on your own. Excellent communication and presentation skills are required.

We invest significantly in both professional and personal development and have an individualised development plan for each employee. Through successful project management and exposure to senior management you will find that Novo Nordisk offers highly attractive career opportunities

At Novo Nordisk, decisions and actions are based on their impact on society, the environment and on their potential to generate a profit. That makes for a responsible culture with a healthy and engaging working environment.

Contact
For further information, please contact Anders Mikkelsen + 45 3079 4461.

Deadline
24 April 2014.

Denmark - Måløv Project Management
10-Apr-2014 GMP Coordinator
Are you interested in working with our broad portfolio of products in Biopharm and help us with our delivery and Quality? In Biopharm Manufacturing Development we are responsible for support to our productions,...

GMP Coordinator

  • Production
  • Denmark - Gentofte

Are you interested in working with our broad portfolio of products in Biopharm and help us with our delivery and Quality? In Biopharm Manufacturing Development we are responsible for support to our productions, transfer of new products from R&D and continuous optimizations of our many processes. You will be a key player in ensuring quality and compliance for Biopharm AP Support consisting of a number of teams. You will be a member of the local Management team and primary sparring partner for the Director and Associate Managers on GMP issues.

About the department
We focus on support to Bioparm AP production, product transfer from R&D and stability of our products. You will have more than 50 highly qualified and motivated colleagues. You will be responsible for GMP and Quality and refer directly to the Director for Biopharm AP Support.

The job
As GMP Coordinator you have the overall responsibility for setting the targets on quality and compliance for your area and for making sure that they will be met. As such, you bring in the latest knowledge within GMP when you challenge our business managers to bring GMP and quality to the top of the agenda. You ensure that the area is in compliance with the authorities’ and Novo Nordisk’s regulations, including ISO9001:2008, and you will become your area’s representative in our cross-organisational GMP group/GMP board. You are also responsible for the departments input to the Quality Management Review (QMR), and you play an active role in audits and inspections. You will participate in our GMP network meetings with your peers for sparring, sharing and development of GMP and QMS related topics. Furthermore, part of the job will be to assist, in the beginning, our Stability team with various tasks and later on other tasks across the department.

The job involves contact and interaction to many different stakeholders in the organisation, from operators, maintenance, LEAN professionals, project managers, and to all line management levels.

Qualifications
You hold a degree at minimum master’s level. Your academic background is topped with experience from a pharmaceutical production company where you have gained solid experience within quality, GMP and ISO9001. You are used to create results through projects and know the importance of team collaboration. To succeed, you must thrive in a role where you take leadership, initiate and coordinate a large number of actions and projects. This requires an excellent overview, a structured mind-set and a dedicated way of working as well as very good communication skills. Working cross-organisationally, your networking skills will also be crucial as well as your ability to balance when to compromise and when to stand firm. Finally, you must master English and Danish, written and spoken.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please call Martin Arendt Petersen on + 45 3079 8228.

Deadline
26 April 2014.

Denmark - Gentofte Production
09-Apr-2014 Internship in CMC DP Business Support
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship in CMC DP Business Support

  • Business Support
  • Denmark - Måløv

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
Novo Nordisk is seeking an engaged student for full time internship to CMC Drug Product (DP) Development Business Support in a period of 6 months. CMC DP Development is part of CMC Supply, which manufacture and distribute drug candidates for pre- and clinical trials, develop commercial manufacturing processes and technologies and produce scientific documentation. CMC DP Development is an organisation with app. 400 employees located in Denmark.

The job
You will be working in a dynamic Business Support team with 8 other dedicated employees in Måløv. The department’s main responsibility is to deliver high quality support to management through ensuring effectiveness and efficiency in business processes, management presentations, performance measurement, balance scorecard process as well as participation in multiple projects.

During your internship your key task will be to deliver high quality support to the team. You will be involved in securing high quality in the monthly performance follow-up as well as participate in cross functional projects. You will be given a unique opportunity to gain a broad insight to the business and key processes. You will get hands-on project management experience in a dynamic environment, working with a dedicated and ambitious team.

Qualifications
You are currently pursuing a Master’s degree in Finance, Business Administration, Engineering or another relevant degree, and have had excellent result during your studies. You pay attention to details and possess good communication skills. Excellent language skills in English and Danish are required.

You like being part of a professional team, have a high energy level, take initiative (proactive thinking) and work with a high level of engagement. You are motivated by being challenged both professionally and personally. You have a flair for IT (Excel and Power Point) and numbers. We expect candidates to be service minded, thrive in a busy environment and bring a can-do attitude. The atmosphere is informal and humorous. If you can hold on to your good sense of humour at all times, you are the kind of person we are looking for.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Practicalities

Qualification: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 6 months.

Start date: 15 August 2014

Contact
For further information, please contact Julie Ebdrup Thomsen on + 45 3079 7359.

Deadline
26 May 2014.

Denmark - Måløv Business Support
09-Apr-2014 Business Analyst
Novo Nordisk is one of the world’s most successful pharmaceutical companies with a great growth potential. Do you want to be part of ensuring that this growth happens in full financial control? ...

Business Analyst

  • Finance
  • Denmark - Bagsværd

Novo Nordisk is one of the world’s most successful pharmaceutical companies with a great growth potential. Do you want to be part of ensuring that this growth happens in full financial control?

About the department
Corporate Financial Planning is part of Corporate Finance (500 employees) and is responsible for the financial management of Novo Nordisk with a close link to the business worldwide. Our aim is to be the best finance operation in the global pharma industry. You will be part of a young and dynamic finance team consisting of 40 dedicated employees split into 6 smaller teams. We have close cooperation with the business units and our aim is to act as true business partners based on strong financial competencies combined with a good understanding of the business in which we operate.

The job
You will be the finance partner for one or more of our business units, including supporting the unit(s) on various financial matters. Our key process related responsibilities are to facilitate the budget process in the areas and provide monthly follow up to senior management. You might also be invited to attend the management meetings as their financial advisor. Furthermore, in order to optimize the financial development within your area of responsibility, you will be involved in various projects and ad hoc analysis.

Qualifications
The person we are looking for has 0-2 years of relevant experience and has completed a relevant master's degree (i.e. in finance or economics) with excellent results. You have strong analytical skills, are computer literate and ready to invest time and effort in your development and future career. Furthermore, it is important that you have good communication skills, including being fluent in written and spoken English as well as being able to communicate with people at all levels of the organisation. The atmosphere in Corporate Financial Planning is informal and humorous. If you can hold on to your good sense of humour at all times, you are the kind of person we are looking for.

We invest a lot in both professional and personal development and have an individualised development plan for each employee. Through on-the-job training, projects and courses you will experience a continued steep learning curve, thus enabling a number of future career opportunities in the global Novo Nordisk organisation.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please contact Kolos Kopcsai on +45 3079 0809.

Deadline
27 April 2014.

Denmark - Bagsværd Finance
09-Apr-2014 Development Engineer
Skilled mechanical engineers! Boost your career in one of the world’s leading companies within medical devices - located in the greater Copenhagen area. Join Device Research & Development at Novo Nordisk A...

Development Engineer

  • Research & Development
  • Denmark - Hillerød

Skilled mechanical engineers! Boost your career in one of the world’s leading companies within medical devices - located in the greater Copenhagen area.

Join Device Research & Development at Novo Nordisk A/S for a life-changing career!

Novo Nordisk A/S, a global healthcare company with 90 years of innovation and leadership in diabetes care, is looking for skilled engineers for mechanical development.

About the department
Device Research & Development, located in Hillerød, is an area within Global Research & Development, responsible for the development of medical devices for self-treatment within all business areas of Novo Nordisk A/S. Device Research & Development has a long and outstanding track-record of developing the best, most innovative and widely-used injection devices in the world. In Device R&D we are determined to develop devices that make a positive difference for our end users whether they are patients, nurses or doctors. You will join a project team of highly skilled engineers and designers, responsible for the development of a new generation injection device to support treatment of chronic diseases.

To learn more about Device Research & Development, please visit: www.novonordisk.com/device-rd

The job
As our new Mechanical System Engineer, you will become a member of mechanical development team that are currently maturing a new device concept for future production.

You will be a part of a cross-functional team and work from the mid to late phases of our product development projects. Your main focus will be to perform system analysis and interface specification, plan and report design verification and validation.

Your contribution will be in all of these areas which entails that your work day is dynamic and rarely the same as the previous. Developing medical devices require a high level of documentation which will be a time consuming task in some periods.

You will be given a number of different responsibilities and experience a variety of tasks, working with both internal and external stakeholders. The job will enhance your professional and personal development, providing you with an opportunity to develop skills within specialist expertise and project management.

Qualifications
You hold an academic degree with at least 5 years of experience within mechanical development. You have worked with mechanical design of plastic components, you master CREO and you are skilled within mechanical disciplines like tolerance stack-ups, material selection as well as kinematic and structural analysis. You have the ability to analyse and understand complex structures and systems.

You are a team player by nature with the ability to work independently with a result-oriented ‘can-do’ attitude. You have a solid academic background with an international profile and must be able to learn fast, excel at cross-functional collaboration and communicate at all levels. You must be prepared to invest significant personal effort in your work and proactively take ownership of your areas of responsibility. You find the role as project coordinator or project manager appealing, and have considered that it might be a future path for you to follow. Proficiency in oral and written English is essential.

At Device Research & Development we use our skills, dedication and ambition to help people with chronic diseases, and change their lives. You will get the opportunity to take part in this, and in addition enhance your career, benefiting from the possibilities for professional and personal development provided by Novo Nordisk A/S.

Device R&D is an organisation with many international employees and we welcome non-local applicants. We have great experience helping people move to Denmark and will support relocation.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please contact Jakob Wielandt on + 45 3075 8881 or Mikkel Larsen on + 45 3075 7410.

Deadline
4 May 2014.

Denmark - Hillerød Research & Development
09-Apr-2014 Training & QC Professional
Are you motivated by coordinating, developing and ensuring training in all Pharmacovigilance aspects, whilst working at a high performance rate? Do you thrive on working with a high level of responsibility, inf...

Training & QC Professional

  • Pharmacovigilance
  • Denmark - Bagsværd

Are you motivated by coordinating, developing and ensuring training in all Pharmacovigilance aspects, whilst working at a high performance rate? Do you thrive on working with a high level of responsibility, influence in Pharmacovigilance training and interaction with many different types of people, at all levels of the organisation?

If you find challenges like this exciting and inspiring, you may be our new Training Professional, securing high quality training in our work to provide the safest products to patients.

About the department
The job is located in a newly established area within Global Safety. Global Safety is globally responsible for handling adverse events, monitoring product safety, customer complaints and potential recalls in Novo Nordisk. The primary responsibilities of the Training and Quality Control department are to ensure that Global Safety is providing Pharmacovigilance training and performing Quality Control on case handling, to ensure that we meet external and internal requirements. We are 10 colleagues with different professional backgrounds, ensuring support to the Qualified Person for Pharmacovigilance in Novo Nordisk. Since our unit is situated in both Bagsværd and India and works with our affiliates across the globe, you will have the opportunity to work with our global colleagues. You can, therefore, expect some travel per year.

The job
You will be responsible for coordinating and developing training material in relevant media and also performing training activities related to Pharmacovigilance, as well as ensuring that training material is up to date and in line with external requirements and internal operating procedures and guidelines. Furthermore, you will be responsible for providing training, tools and techniques to ensure documented training efficacy. This also implies Affiliate visits.

You will be expected to ensure coherence between requirements and internal operating procedures and guidelines, as well as participating in cross-functional projects.

Other responsibilities include maintenance of all metrics related to these processes, trending and analysis of reports produced in the department, including writing executive summaries and conclusions based on your analysis.

You will be expected to have a good collaboration and interaction with our stakeholders, which range from staff throughout Global Safety to the clinical, regulatory areas and affiliates.

Qualifications
You hold a Master’s degree with a scientific background, e.g. Medical, Chemistry, Biology, Pharmacy and Engineering and have documented experience within training as well as project management. It is an asset that you have broad Pharmacovigilance experience. You have excellent written and oral communication abilities in English. You are open-minded, enthusiastic and possess the ability to work independently and internationally and drive your job responsibilities. You have good cooperation skills, a high degree of flexibility and are used to delivering according to targets. The role requires analytical skills and a strong quality orientation, including the ability to focus on details and adherence to standards, whilst maintaining a balanced business perspective.

At Novo Nordisk we use our skills, dedication and drive to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please contact Mette-Marie T. Nøigaard on +45 3079 4462.

Deadline
24 April 2014.

Denmark - Bagsværd Pharmacovigilance
08-Apr-2014 Experienced Senior Quality Professional
Do you want to influence a high level of compliance with GMP / quality management system (QMS) requirements, ISO standards and Novo Nordisk procedures? Then you might be the right person for the job as Senior Q...

Experienced Senior Quality Professional

  • Quality, senior position
  • Denmark - Hillerød

Do you want to influence a high level of compliance with GMP / quality management system (QMS) requirements, ISO standards and Novo Nordisk procedures? Then you might be the right person for the job as Senior Quality Officer in Device Manufacturing & Sourcing (DMS).

About the department
As our Senior Quality Officer you will be part of our QMS support team in DMS. The team reports directly to the Quality VP in DMS. The team is responsible for cross functional quality activities in DMS, such as coordination and follow-up on audits and inspections, GMP training, reporting on quality KPI’s, QMR and the CAPA system. The team provides cross functional QA services and coordinates quality assurance initiatives and projects.

The job
You will play a key-role in setting directions and standards for the way DMS implements and maintains continuous improvements and harmonisations into the QMS as well as drive or participate in quality projects and initiatives coming out of our Product Supply organisation to ensure an effective implementation in DMS.

You will be part of DMS Quality management team and also provide QMS support to DMS management. It is your responsibility to report and follow-up on quality activities and topics at monthly management meetings and you will be Process Responsible for one or more quality processes e.g. the QMR process and GMP training, with a direct possibility to influence the compliance level in DMS.

Ensuring a high level of inspection readiness you are responsible for coordination, execution and support follow-up on audits and inspections.

Further, it is your responsibility to ensure compliance alignment and knowledge sharing between DMS and our Product Supply organisation by participating in QA cross and compliance groups as DMS representative.

Qualifications
You hold an academic degree as engineer or pharmacist and have preferable +5 years of experience from a pharmaceutical or medical device industry where you have gained a solid and up-to-date knowledge of quality, GMP and ISO requirements. It is important that you have an in-depth understanding of QMS requirements and have been working with interpretation, implementation and training in new QMS requirements. Further, we expect you to have experience as lead auditor and with project management.

As a person you are enthusiastic, committed and proactively seek the information you need and have hands on approach. You are analytical and systematic in your approach. You are able to see things in larger perspectives and experienced in working and communicating with people at all levels in the organisation and across organisational boundaries. You use your excellent cooperation skills when you manage your stakeholders both in- and externally to ensure solutions that will meet both requirements and stakeholders’ interest.

You are service-minded, enterprising, independent and persistent. In DMS we are determined to be best in class and it is therefore important that you are able to see opportunities instead of limitations without compromising a high level of compliance.

Finally, you communicate fluently both written and spoken in English.

At Novo Nordisk, decisions and actions are based on their impact on society, the environment and on their potential to generate a profit. That makes for a responsible culture with a healthy and engaging working environment.

Contact
For further information, please call Jacob Stenmann Valsborg at +45 3075 4798.

Deadline
21 April 2014.

Denmark - Hillerød Quality, senior position
08-Apr-2014 Senior Risk Advisor
Would you like to drive enterprise risk management in a truly global organisation? Do you strive on combining cross-functional business understanding with financial acumen to identify and scope organisational c...

Senior Risk Advisor

  • Finance
  • Denmark - Bagsværd

Would you like to drive enterprise risk management in a truly global organisation? Do you strive on combining cross-functional business understanding with financial acumen to identify and scope organisational challenges and develop solutions? Do you have a flair for providing high quality business support to and interacting with stakeholders at Senior Management level? If so, this position may be what you are looking for!

About the Department
The Risk Office, located as part of the Corporate Financial Planning, is the secretariat of the Risk Management Board, consisting of Senior Management and chaired by the CFO. We are a young and dynamic team of four, responsible for driving Novo Nordisk’s Enterprise Risk Management system, and we are currently looking for a Senior Risk Advisor who can bring relevant experience and insight to help us continue delivering superior business support to our organisation and stakeholders.

The job
You will be responsible for driving the overall ERM system and the quarterly risk reporting process in your areas of responsibility. This will require you to work closely with different parts of the organisation to ensure that relevant risks are identified and assessed, and act as a sparring partner. To accomplish this task successfully, you will be required not only to have a profound understanding of the value chain activities, but also to utilise it actively to raise relevant discussions on risk content and bring insights to different stakeholders.

You will also be responsible for conducting and facilitating relevant risk workshops with Senior Management teams and other stakeholders. This is a crucial task that allows us to maintain momentum in the risk organisation and secure strong risk anchoring.

Finally, you will drive and contribute to a variety of interesting risk projects, which are normally carried out in cooperation with stakeholders and colleagues from a variety of organisational functions and aim at supporting and enhancing different parts of the ERM system and/or risk reporting process.

In the Senior Risk Advisor role, you will gain excellent insight into the global Novo Nordisk organisation and will get an opportunity to work on truly cross-functional projects. You will also be exposed to all activities in the Novo Nordisk global value chain, which will enable you to develop unique business understanding and establish a broad network in the organisation.

You will be physically located in the Novo Nordisk headquarters in Bagsværd, Denmark. However, some international travel will be required.

Qualifications
You hold a master’s degree in business, chemistry, supply chain, production, quality, engineering or similar, and your career so far has provided you with in-depth experience and knowledge related to your area of expertise. You possess strong analytical and strategic thinking capabilities, and can solve complex problems fast.

You have strong facilitation, communication/presentation and stakeholder engagement skills and connect easily with others. In this job, solid interpersonal and leadership skills are a must, and so is intercultural awareness and sensitivity.

Last but not least, you have a sense of humour and are praised by your peers as a dedicated and hard-working colleague. You are fluent in spoken and written English, and have strong PC skills (incl. MS Office).

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Contact
For further information, please call Annette Fiig on + 45 3079 6962.

Deadline
27 April 2014

Denmark - Bagsværd Finance
08-Apr-2014 QA Chemist
Would you like to help securing release of Novo Nordisk A/S Glucagon? Do you thrive when working in a team; handling multiple tasks of high complexity? Then you might be the person we are looking for in Biophar...

QA Chemist

  • Quality
  • Denmark - Gentofte

Would you like to help securing release of Novo Nordisk A/S Glucagon? Do you thrive when working in a team; handling multiple tasks of high complexity? Then you might be the person we are looking for in Biopharm QA Aseptic Production.

About the department
Biopharm QA AP is responsible for quality assurance of three existing aseptic filling plants and the building of a new filling plant, two laboratories and all utility systems in the Gen-tofte production areas. Our key tasks are to review and approve all sorts of GMP docu-mentation such as validation reports, change requests and non-conformities and batch documentation in order to be able to release filled product for packaging.

As QA Chemist in Biopharm QA AP you will join a group of highly skilled and competent colleagues working in five teams lead by separate associate managers. By joining us you will get the chance of professional and personal development and you will get an excellent and unique overview of current authority expectations and demands in the pharmaceutical industry.

The job
The position is situated in Gentofte in one of our releasing teams for filling plants. The team consists of 12 chemists. The job includes QA review of several types of documents hereunder batch documentation to ensure release of Glucagon. The documents come from all types of processes thus guaranteeing a high level of variety on a daily business.

Your main responsibility will be to quality assure the release of Glucagon. And thereby contribute to assure product quality and compliance with the current GMP rules and guidelines. On top of that QA is a major player at internal audits and external authority inspections, where you are expected to participate.

When started you will undergo an individual and intense training program, where you can expect to be given more responsibility gradually.

Qualifications
You hold an academic degree that qualify you as QP (Qualified Person) according to the Danish Medical Agency. Preferable your academic background is topped with experience either from the pharmaceutical industry. However we would also like to hear from talent-ed newly academic graduates.

It is important that you thrive in a role where you are required to take independent deci-sions and show a high degree of authority. You have a strong quality mind-set and you are robust. You know and meet your deadlines and you are capable of prioritising between different tasks in a dynamic environment. You are a dedicated team player who inspires trust and respect amongst colleagues and partners. Your language skills cover proficiency in both Danish and English.

Your application is welcome in Danish or English.

Contact
For further information, please contact Rune Goldschmidt Ruders at +45 3075 5361 or Rikke Wissing Jensen at +45 3075 1566.

Deadline
25 April 2014.

Denmark - Gentofte Quality
08-Apr-2014 QA Chemist
Would you like to help securing release of Novo Nordisk A/S products from different pro-duction facilities in Gentofte? Do you thrive when working in a team; handling multiple tasks of high complexity? Then you...

QA Chemist

  • Quality
  • Denmark - Gentofte

Would you like to help securing release of Novo Nordisk A/S products from different pro-duction facilities in Gentofte? Do you thrive when working in a team; handling multiple tasks of high complexity? Then you might be the person we are looking for in Biopharm QA Aseptic Production.

About the department
Biopharm QA AP is responsible for quality assurance of three existing aseptic filling plants and the building of a new filling plant, all utility systems in the Gentofte production areas and all equipment and facility qualification activities. Our key tasks are to review and ap-prove all sorts of GMP documentation such as change requests, non-conformities, valida-tion and qualification protocols and reports (IQ, OQ, PQ) in order to secure a stable plat-form for the continuous release of filled product.

As QA Chemist in department Biopharm QA AP you will join a group of highly skilled and competent colleagues working in four teams lead by separate associate managers. By joining us you will get the chance of professional and personal development and you will get an excellent and unique overview of current authority expectations and demands in the pharmaceutical industry.

The job
The position is situated in Gentofte and the team consists of 12 chemists. The job includes QA review of several types of documents with special focus on qualification activities regarding production equipment and facility. The documents come from all types of processes thus ensuring a high level of variety on a daily basis.

Your main responsibility will be to quality assure qualification activities hereunder instal-lation and operational qualification. Thereby contribute to assure product quality and compliance with the current GMP rules and guidelines. On top of that QA is a major player at internal audits and external authority inspections, where you are expected to partic-ipate.

When started you will undergo an individual and intense training program, where you can expect to be given more responsibility gradually.

Qualifications
You hold an academic degree as an engineer, pharmacist or alike. Preferable your aca-demic background is topped with qualification experience from the pharmaceutical indus-try. However, we would also like to hear from talented newly academic graduates.

It is important that you thrive in a role where you are required to take independent deci-sions and show a high degree of authority. You have a strong quality mind-set and you are robust. You know and meet your deadlines and you are capable of prioritising between different tasks in a dynamic environment. You are a dedicated team player who inspires trust and respect amongst colleagues and partners. Your language skills cover proficiency in both Danish and English.

Your application is welcome in Danish or English.

Contact
For further information, please contact Rune Goldschmidt Ruders at +45 30755361 or Rikke Wissing Jensen at +45 3075 1566.

Deadline
25 April 2014.

Denmark - Gentofte Quality
08-Apr-2014 Corporate Process Expert for the Quality Risk Management process
Do you possess experience and in-depth knowledge within Quality Risk Management? Do you have a proven record in planning and delivery of process improvements? Can you take a corporate leadership and are you use...

Corporate Process Expert for the Quality Risk Management process

  • Quality
  • Denmark - Bagsværd

Do you possess experience and in-depth knowledge within Quality Risk Management? Do you have a proven record in planning and delivery of process improvements? Can you take a corporate leadership and are you used to communicate complex issues in an easily understandable way? - then go for this job!

About the department
Quality Capability Development (QCD) is part of the Corporate Quality organisation in Novo Nordisk. We are a small team of process experts responsible for ensuring compliance to external requirements and continuously improving a number of quality processes under our responsibility to the benefit of all our stakeholders in Novo Nordisk. The department is located in Bagsværd, Denmark.

The Job
As the Quality Risk Management (QRM) Process Expert in Novo Nordisk, your primary job will be to ensure that Novo Nordisk stays in compliance with external requirements, to set strategic direction for the QRM process, to continuously improve the way we work, to communicate relevant issues at all levels in the organisation and to secure more efficient and effective processes across Novo Nordisk globally. As the corporate Process Expert you will establish and drive a small network of local QRM experts from LoB. Your role will be to ensure development of QRM operational standards, prepare and describe tools and guidance, deliver training including the QRM Facilitator training programme, prepare and deliver a process strategy, establish process KPIs and follow-up on process performance etc. You will furthermore be expected to deliver compliance support within QRM to LoB e.g. during audits and inspections.

In Novo Nordisk we are currently strengthening our process orientation and you will be a key player in implementing and maturing the process management in the QRM process in close cooperation with the Process Owner Delegate.

Qualifications
You have an academic background e.g M.Sc. and a solid and up-to-date experience within QRM. It is important that you have an in-depth understanding of QRM related external requirements and hands-on experience with interpretation, implementation and practices most likely from some years of experience in a Pharmaceutical or Medical Device company. You may have a formal Project Manager education, but more importantly you have a proven record of driving continuous improvements activities to implementation in an international organisation and as such have the needed competencies to impact the organisation at all levels. You are an enthusiastic and committed person with personal assertiveness and ability to take leadership and motivate others. You are experienced in working and communicating with people at all levels in the organisation. You are required to communicate fluently in English and preferably in Danish and you must be able to present complex matters in a simple way. You are service-minded, enterprising, independent and persistent. We are determined to continuously improve our work and it is therefore important that you are able to see opportunities instead of limitations and can achieve results.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For additional information, please contact Mette Fjord Andersson on + 45 3079 4692.

Deadline
11 May 2014.

Denmark - Bagsværd Quality
08-Apr-2014 QA Project Manager
Do you want to be a part of assuring that Novo Nordisk A/S is developing products of high quality. Are you interested in working with quality of new products?The project portfolio is increasing, and therefore w...

QA Project Manager

  • Project Management
  • Denmark - Gentofte

Do you want to be a part of assuring that Novo Nordisk A/S is developing products of high quality. Are you interested in working with quality of new products?The project portfolio is increasing, and therefore we are looking for a dedicated, professional and enthusiastic new colleague. The QA Project Manager has a unique position that requires interactions with all areas involved in development of new product candidates and as QA Project Manager you will have the chance to support the entire process for development of Novo Nordisk’s new products.

About the department
CMC Project Planning and Management QA (CMC PPM QA) is a central unit in CMC QA with the responsibility for project management of CMC quality assurance activities for the entire Novo Nordisk portfolio of development projects. We are managing the projects from research to launch, while ensuring optimal collaboration across CMC QA as well as Product Supply QA. We are approx. 13 highly skilled and dedicated employees, 9 QA project manager and 3 quality support employees. The department is organised in R&D and located in Gentofte (Bagsværd). Our mission is to act as one point of entry for R&D Projects, ensuring that quality activities are planned and fulfilled according to company policies, and be driver of solving quality issues.

The job
As a project manager in CMC QA you will be working in an engaging and challenging environment. You will be a part of a small project management team – 9 employees that are driving the QA activities in the development projects.

Your main task is to ensure the quality in one or more development projects and coordinate all QA activities related to the CMC activities. You will be the CMC QA representative in the CMC Development core group and will work closely with the CMC project manager. You will act as advisor in quality matters and be the driver of solving quality issues. You will establish and lead relevant QA-groups consisting of professionals performing QA activities. You will be responsible for ensuring that quality activities are planned and fulfilled according to company policies.

It is important that you thrive by communicating with stakeholders and understand the importance of timeliness, structured working methods and thorough documentation. Improvement tools such as LEAN and Quality Risk Management will be part of your daily work.

Qualifications
M.Sc or PhD in pharmacy, engineering, biology or chemistry and thorough practical work experience with cGMP. Experience with project management in the pharmaceutical industry is an advantage.

A broad background and experience from more than 5 years employment comprising pharmaceutical development and/or pharmaceutical production is necessary in this job. Excellent English skills are a prerequisite.

We expect you to have a strong quality mindset and excellent communication skills and that you adapt easily to a changing environment and priorities. You have a well-structured approach to your tasks and are capable of maintaining an overview when under pressure. You have a high level of responsibility, flexibility, independence and initiative. You never loose focus, despite changing demands, priorities or tight deadlines.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information please contact Eva de Bang on + 45 3079 1297.

Deadline
20 April 2014.

Denmark - Gentofte Project Management
08-Apr-2014 Internship
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship

  • Marketing
  • Denmark - Køge

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

About the department
This is an exciting opportunity to join an international, high performing team in Køge, Denmark. You will work with the marketing department in the implementation of the 2014 marketing initiatives. You will work in close collaboration with the sales organization in ensuring we establish the correct strategies and approach in the market.

The job
You will assist the marketing communication team targeting key global. In this role you will perform targeted literature searches to address strategic questions, help to develop/ensure timely updates to our internal tools, work with team members to develop new marketing strategies, and assist with value communication planning/development. E.g. Flyers design, Newsletter support, Market data evaluation, Market research, plus the ability to create content for all marketing material.

Qualifications
You are a university student in Life sciences with focus on Biopharmaceuticals with a scientific knowledge of the cell culture media.

You are currently studying on your master’s degree in Life sciences and have a deep knowledge of the cell culture media. We expect candidates to be service minded, thrive in a busy environment and bring a can-do attitude. Fluency in both oral and written English, sound personal judgment, and excellent interpersonal skills are required.

You are an outgoing person with a strong personal drive and dedication. You have professional and personal impact that is reflected in your desire to take initiative. In addition, you thrive in a busy environment and bring a can-do attitude and a healthy sense of humour to your work – even when the pressure is on. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

Practicalities
Students in their first or second year of their master studies. The internship position is a full-time position for 6 months.

Contact
For further information, please call Vanessa Leon on +45 5667 1091

Deadline
2 June 2014

Denmark - Køge Marketing
08-Apr-2014 Drug Product Coordinator
Are you looking for new challenges within formulation, process or analytical method development of solid dosage forms and do you want to make a difference? Our Oral Protein Formulation Unit (OPF) in Måløv is ex...

Drug Product Coordinator

  • Research & Development
  • Denmark - Måløv

Are you looking for new challenges within formulation, process or analytical method development of solid dosage forms and do you want to make a difference? Our Oral Protein Formulation Unit (OPF) in Måløv is expanding therefore we are looking for several dedicated, professional and enthusiastic new colleagues. Novo Nordisk is on a voyage towards the development and production of oral formulations of proteins. Our ambition is to develop break-through products based on orally available versions of insulin and GLP-1. You will be involved in CMC activities for formulation/process development, pilot production, scale-up and analysis of solid protein dosage forms towards clinical trials.

About the department
We are 26 scientists and technicians in Oral Formulation & Process Development organized in two teams. The Department is overall responsible for development of Solid Dosage Forms of Insulin and GLP-1 molecules for oral delivery. The formulation development covers from early phase development of oral protein formulations and processes in small scale to later stages of formulation development with larger scale. In the later phase the progress towards robust manufacturing processes is of critical importance. The formulation development is done using rational design, statistical and QBD principles.

The job
We are looking for an experienced Drug Product Coordinator to coordinate oral product portfolio projects.

As a Drug Product Coordinator you will be responsible for aligning the project organisation needs with those of the Line of Business. You will be part of the cmc core project team along with the other technical coordinators e.g. API and analysis as well as collaborate closely with the departmental oral product development groups. In this dual role you will define specific department activities linked to the overall project key deliverables. Close collaboration with the line management of the departments is vital in order to ensure the most optimal planning and execution of project targets.

More detailed responsibilities include: Breakdown of project key deliverables to department activities in our primary project planning system. Plan the timing of department activities together with department team leaders and other project coordinators. Communicate risk based development and pilot manufacture scenarios to the project core group. Clear and timely communication of project requirements to team and department members. Prepare and coordinate regulatory documentation according to international guidelines. Drive continuous improvements using LEAN/Six Sigma approach.

Qualifications
The person we are looking for ideally has 3-5 years of experience in managing CMC activities covering early to late phase clinical development. Detailed knowledge of the pharmaceutical value chain is a must as well as excellent knowledge of the CMC documentation flow.Scientific experience with Solid Dosage Form drug development and manufacture is a great advantage for the candidate as is knowledge in protein analysis, characterization and formulation

A MSc or PhD education level in a relevant scientific field is compulsory in order to become a successful applicant for the position.

As a person we expect you to have excellent collaboration skills, be structured and reliable and to have an ability to keep your cool and make the right decisions in a hectic work environment. Also, you are a team player and have a feel for communicating essential information to the right stakeholders at the right time.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information please contact Lone Løgstrup Kimer at +45 3079 3569.

Deadline
30 April 2014.

Denmark - Måløv Research & Development
07-Apr-2014 Senior Formulation Scientist - Solid Dosage Forms
Are you looking for new challenges within formulation, process or analytical method development of solid dosage forms and do you want to make a difference? Our Oral Protein Formulation Unit (OPF) in Måløv is ex...

Senior Formulation Scientist - Solid Dosage Forms

  • Research & Development
  • Denmark - Måløv

Are you looking for new challenges within formulation, process or analytical method development of solid dosage forms and do you want to make a difference? Our Oral Protein Formulation Unit (OPF) in Måløv is expanding therefore we are looking for several dedicated, professional and enthusiastic new colleagues. Novo Nordisk is on a voyage towards the development and production of oral formulations of proteins. Our ambition is to develop break-through products based on orally available versions of insulin and GLP-1. You will be involved in CMC activities for formulation/process development, pilot production, scale-up and analysis of solid protein dosage forms towards clinical trials.

About the department
We are 26 scientists and technicians in Oral Formulation & Process Development organized in two teams.. The Department is overall responsible for development of Solid Dosage Form of Insulin and GLP-1 molecules for oral delivery. The formulation development covers from early phase development of oral protein formulations and processes in small scale to later stages of formulation development with larger scale. In the later phase the progress towards robust manufacturing processes is of critical importance. The formulation development is done using rational design, statistical and QBD principles.

The job
Overall, you will play a key role in expanding our competency base within the Solid Dosage Form process technology area. This involves providing scientific knowledge for maintaining and building the competencies and technology necessary to go from early research laboratory scale through pilot up-scaling within Solid Dosage Forms. You will be responsible for developing and documenting oral protein formulations and processes for preclinical evaluation and early clinical trials. As part of the process development team, your main task is to set up and report experimental designs to develop oral protein formulations as well as the processes.

More detailed responsibilities include: Drive risk management of projects in the product development team and report risk based scenario results to project core group. Plan and execute project tasks according to a DOE setup. Daily collaboration with technicians, as well as technical supervision in laboratories. Prepare technical protocols and reports and compile technical transfer documents for clinical trial pilot production. Give input to Master Batch Records, IMPDs, and related regulatory documents. Support Pilot production team during GMP production and drive continuous improvements using LEAN/Six Sigma approach.

With your experience from the pharmaceutical industry, you represent the department in multidisciplinary project groups, in which you work closely with experts from a wide range of areas.

Qualifications
The ideal candiate, has a PhD in Pharmacy, Engineering, Chemistry or a related field of study and at least 2 years of experience from the pharmaceutical industry. Alternatively, you have a Master’s degree and at least 5 years of experience with the formulation and process optimisation of Solid Dosage Forms e.g. within mixing, granulation, compression, coating, or pharmaceutical-technical analyses. You enjoy working in a dynamic environment, where teamwork is at the top of the agenda. As a person, you are known for a high commitment to finding constructive solutions as well as taking responsibility for your assignments.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please call Thomas Lundberg Rand on + 45 3075 8448 or Lone Løgstrup Kimer on + 45 3079 3569.

Deadline
24 April 2014.

Denmark - Måløv Research & Development
07-Apr-2014 Senior formulation scientist - Solid Dosage Forms
Are you looking for new challenges within formulation, process or analytical method development of solid dosage forms and do you want to make a difference? Our Oral Protein Formulation Unit (OPF) in Måløv is ex...

Senior formulation scientist - Solid Dosage Forms

  • Research & Development
  • Denmark - Måløv

Are you looking for new challenges within formulation, process or analytical method development of solid dosage forms and do you want to make a difference? Our Oral Protein Formulation Unit (OPF) in Måløv is expanding therefore we are looking for several dedicated, professional and enthusiastic new colleagues. Novo Nordisk is on a voyage towards the development and production of oral formulations of proteins. Our ambition is to develop break-through products based on orally available versions of insulin and GLP-1. You will be involved in CMC activities for formulation/process development, pilot production, scale-up and analysis of solid protein dosage forms towards clinical trials.

About the department
We are 26 scientists and technicians in Oral Formulation & Process Development organized in two teams.. The Department is overall responsible for development of Solid Dosage Form of Insulin and GLP-1 molecules for oral delivery. The formulation development covers from early phase development of oral protein formulations and processes in small scale to later stages of formulation development with larger scale. In the later phase the progress towards robust manufacturing processes is of critical importance. The formulation development is done using rational design, statistical and QBD principles.

The Job
Overall, you will play a key role in expanding our competency base within the Solid Dosage Form process technology area. This involves providing scientific knowledge for maintaining and building the competencies and technology necessary to go from early research laboratory scale through pilot up-scaling within Solid Dosage Forms. You will be responsible for developing and documenting oral protein formulations and processes for preclinical evaluation and early clinical trials. As part of the process development team, your main task is to set up and report experimental designs to develop oral protein formulations as well as the processes.

More detailed responsibilities include: Drive risk management of projects in the product development team and report risk based scenario results to project core group. Plan and execute project tasks according to a DOE setup. Daily collaboration with technicians, as well as technical supervision in laboratories. Prepare technical protocols and reports and compile technical transfer documents for clinical trial pilot production. Give input to Master Batch Records, IMPDs, and related regulatory documents. Support Pilot production team during GMP production and drive continuous improvements using LEAN/Six Sigma approach. With your experience from the pharmaceutical industry, you represent the department in multidisciplinary project groups, in which you work closely with experts from a wide range of areas.

Qualifications
The ideal candiate, has a PhD in Pharmacy, Engineering, Chemistry or a related field of study and at least 2 years of experience from the pharmaceutical industry. Alternatively, you have a Master’s degree and at least 5 years of experience with the formulation and process optimisation of Solid Dosage Forms e.g. within mixing, granulation, compression, coating, or pharmaceutical-technical analyses. You enjoy working in a dynamic environment, where teamwork is at the top of the agenda. As a person, you are known for a high commitment to finding constructive solutions as well as taking responsibility for your assignments.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information please contact Thomas Lundberg Rand on +45 3075 8448 or Lone Løgstrup Kimer on +45 3079 3569.

Deadline
24 April 2014.

Denmark - Måløv Research & Development
07-Apr-2014 Data Manager Specialist
Are you interested in working with Electronic Data Capture, Clinical Data Management System, clinical standards and biological data? Do you want to be a key player in the drug development process? Do you like t...

Data Manager Specialist

  • Research & Development
  • Denmark - Søborg

Are you interested in working with Electronic Data Capture, Clinical Data Management System, clinical standards and biological data? Do you want to be a key player in the drug development process? Do you like to work with leading technology and processes? Do you like a challenging and rewarding workplace? Do you like having a broad and daily contact with colleagues and partners from around the globe? Then a role in the DM Operations department of 40 data managers is for you.

About the department
DM Operations is responsible for ensuring the many systems we use for collecting data for our trials are correctly linked so as there is a proper and timely flow of data to our Clinical Data Warehouse. Our department is working closely with internal as well as external partners. We are seeking a new colleague to take up the position as Data Manager Specialist. The working place will be our office building in Søborg.

The job
You will work closely with other Data Management colleagues from around the globe as well as be an integral part of the trial study team. The Data Manager Specialist in the DM Operations dept. is primarily responsible for the coordination and timely set-up of DM systems, project standards and mulitiple trial deliverables during conduct and closure. The job requires a strong knowledge of Oracle Clinical, ePRO systems, CDISC, InForm and relational databases is required. Furthermore strong project planning and project management skills are necessary. It is expected that you can handle all trial related documentation as well as have a strong understanding of how the data is used by our statistical programmers and statisticians. As Data Manager Specialist, understanding, utilizing and communicating best practice methodologies will be a part of your daily work tasks. As Data Manager Specialist you are expected to be an expert in data management from trial build to trial closure and share this expertise with your colleagues.

Qualifications
You have a B.Sc. or M.SC within IT, natural sciences or other relevant degree and extensive knowledge and experience from the Pharma industry, GCP knowledge. You have excellent overview, presentation and coordination skills. Furthermore, good English skills, strong cooperation and analytical skills are a necessity. You are capable of working independently, take on responsibility and show initiative. We expect you to be able to overview several tasks in parallel without compromising the quality of your work and that you remain high spirited, also when things are moving fast. You have very good communication skills and can navigate successfully in a global environment. Relevant experience in dealing with clinical data domains in the pharmaceutical industry is required - preferably minimum 8 years. You will be offered a competitive remuneration package together with on-going training and development in a professional and supportive working environment.

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Contact
For further information, please call Elinor Løbner-Olesen on + 45 3079 2845 or Ellen Sørensen on + 45 3075 5588.

Deadline
16 April 2014.

Denmark - Søborg Research & Development
07-Apr-2014 Sr. Project Coordinator
We are currently looking for a Project Coordinator with an interest in and experience with, the development of the design of printed packaging materials, and coordination of labelling launch activities. ...

Sr. Project Coordinator

  • Regulatory Affairs
  • Denmark - Søborg

We are currently looking for a Project Coordinator with an interest in and experience with, the development of the design of printed packaging materials, and coordination of labelling launch activities.

About the department
Labelling Development and Launch is part of Regulatory Affairs, which makes medicine available to patients all over the world by ensuring rapid regulatory approval in all markets.

You will join nineteen skilled and motivated colleagues in Regulatory Labelling Development and Launch. The department is responsible for the printed packaging material development and launch projects. We drive the development of printed packaging material designs for all new Novo Nordisk products and life cycle management projects, and we ensure timely market launch of printed packaging materials for all Novo Nordisk products globally. The permanent position is located in Søborg, Denmark.

The job
As a Project Coordinator your primary task will be to independently drive and coordinate projects, both with regards to secondary packaging development and launch activities.

Your job will be to set the right direction for the project and, at the same time, ensure that your project is implemented and anchored in the organisation. The projects will vary in size and complexity, but will all be cross-organisational. You will ensure delivery of results on both printed packaging material projects and launch activities according to the overall project plans. You will be responsible for thoroughly creating, storing, and archiving the relevant documentation for project activities and decisions according to Good Documentation Practices and internal procedures. You will work together with many stakeholders on a cross functional level.

Qualifications
You have completed a relevant Master's Degree (Masters of Science, Engineering, or other) with excellent results, and have at least 3 years’ experience from the pharmaceutical industry. You have acquired solid experience within project management. You are comfortable interacting with stakeholders at any organisational level and are used to working across organisational and geographical boundaries. Leading others in project contexts comes natural to you, and you use your energy and understanding of other people to involve the right competencies in the right processes and carry projects ideas through with success. Development of packaging material is a fast moving field where new requirements constantly emerge. Therefore the position requires a good understanding of e.g. design controls and human factors engineering.

You are able to work very independently and have a high level of drive, initiative and persistence. You are result-oriented, ambitious, and like to be challenged. You are analytical, structured and comfortable managing a team on your own. You are proficient in Office applications. An excellent command of our corporate language, English, is a must, and knowledge of Danish is an advantage.

In Novo Nordisk it is your skills, your commitment and your ambitions, which helps us improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer our employees opportunities for continuous growth.

Contact
If you have any questions about the position, please contact Bente Jessen on +45 3075 8056.

Deadline
25 April 2014.

Denmark - Søborg Regulatory Affairs
04-Apr-2014 Category Management
Do you have a strong business mind-set and are you looking for a job with the possibility to establish or further develop your skills and competences within category management, market and spend analysis, stake...

Category Management

  • Sourcing
  • Denmark - Bagsværd

Do you have a strong business mind-set and are you looking for a job with the possibility to establish or further develop your skills and competences within category management, market and spend analysis, stakeholder management, negotiations and contracting?

About the department
Corporate Procurement is, in close cooperation with affiliates and stakeholders, responsible for purchasing, sourcing and contracting of the global indirect spend in Novo Nordisk. Corporate Procurement has more than 100 employees and is anchored in the Corporate Finance organisation. You will be part of the Meetings & Events group in our Marketing, Professional & Travel Management Services Department, which is responsible for categories within marketing services related to the pharmaceutical industry, travel services, management and business consulting, company cars, financial services and legal services.

The Job
As Associate Category Manager you will have a variety of tasks. On an operational level you will act as commercial anchor-point responsible for leading structured sourcing and negotiation processes including: supporting creation of a pipeline of projects, conducting structured tender processes in accordance with the standard Novo Nordisk sourcing model and establishing strong stakeholder relationships across the global organisation.. On larger projects you will team up with senior colleagues to support you professionally and to drive your personal development

You will also be involved in establishment and implementation of category strategies including: business and market intelligence facilitating fact-based decision making, incl. development of cost models, excellent supplier relationship management, and ensuring value creation for different business areas across Novo Nordisk in line with category strategies.

Qualifications
We expect you to have a relevant Master degree with excellent results. Most importantly you have solid business acumen.

The ideal candidate has 1-5 years working experience. A good understanding of strategic sourcing of professional services will be an advantage. Further, the ideal candidate has experience from or interest in negotiation of both specific delivery contracts and frame agreements. You possess a combination of project management and strong analytic capabilities, together with excellent people skills. You are able to advise senior stakeholders on best sourcing practices as well as on commercial aspects during negotiations.

As a person you are ambitious and a proactive self-starter driven by achieving the best possible results while acting in a responsible and ethical way. You are a well-liked colleague and a team player. You easily establish a high level of trust and commitment with colleagues, stakeholders and suppliers. Your ability to connect and relate to internal stakeholders is a key competency, and a proven track record from a larger organization is an advantage.

My opportunities At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please contact Peter Dam Madsen on +45 3079 3226.

Deadline
22 April 2014.

Denmark - Bagsværd Sourcing
04-Apr-2014 Team Leader
Are you interested in working in an international and challenging environment where you can use your managerial and DM skills? Are you interested in working with Clinical Data Management System, clinical standa...

Team Leader

  • Research & Development
  • Denmark - Søborg

Are you interested in working in an international and challenging environment where you can use your managerial and DM skills? Are you interested in working with Clinical Data Management System, clinical standards, biological data and project management? Then a role in the DM Operations department of 40 data managers is for you.

We are looking for a new Team Leader for one of our sub-departments. We are part of the Global Development organisation who is responsible for transforming promising new drug candidates into effective treatments for patients.

About the department
DM Operations is responsible for ensuring the many systems we use for collecting data for our trials are correctly linked so as there is a proper and timely flow of data to our databases. Our department is working closely with internal as well as external partners locally and internationally. The working place will be our office building in Søborg. We have a good work environment with focus on diversity, cooperation and personal development.

DM Operations supports several stakeholders both within and outside Global Development and has a strong focus on upholding high quality and timely deliveries, which are key since we support an essential part of clinical drug development in Novo Nordisk.

The job
As Team Leader you will be responsible for day to day management of a team of 10–15 data managers working in the insulin therapeutic area, providing leadership, direction and prioritisation as necessary for the unit. You will coach, mentor and develop the team in alignment with business needs and Novo Nordisk Way.

You will also take up various ad-hoc tasks and/or projects so good project management skills are a requirement.

Qualifications
You have a good understanding of the clinical development process within the pharmaceutical industry and flair for project management and IT. You understand the regulatory requirements associated with data collected in clinical systems and can transform this to support the business.

You have minimum 5 years of experience with clinical trial conduct and preferably 2 years’ experience with project or line management. In addition you possess a profound knowledge of drug development and computer systems/IT. You also have experience with development of clinical standards and knowledge of external standards and collaboration across professional and regional borders. As a person you are out-going, motivated, and enthusiastic and have the power to influence. You are adaptable with a flexible attitude, both regarding organisation, staff and environment. We also expect that you are honest, committed and responsible as well as an organisational talent including being efficient and systematic.

The position is based in Clinical Systems & Data Management in Søborg, Denmark. Some travelling is expected due to engagement with stakeholders around the world e.g. affiliates and vendors.

At Novo Nordisk, we use our skills, dedication and ambition to help people with diabetes. We offer the chance to be part of a truly global work place, where passion and engagement are met with opportunities for professional and personal development.

Contact
For further information, please call Elinor Løbner-Olesen on + 45 3079 2845.

Deadline
22 April 2014.

Denmark - Søborg Research & Development
04-Apr-2014 GCC Coordinator
Do you want to join a department of highly engaged colleagues working with Novo Nordisk clinical research activities worldwide. Then you might be the right person for the job as GCC Coordinator in the Global Cl...

GCC Coordinator

  • Administrative
  • Denmark - Søborg

Do you want to join a department of highly engaged colleagues working with Novo Nordisk clinical research activities worldwide. Then you might be the right person for the job as GCC Coordinator in the Global Clinical Compliance Department in R&D Quality.

About the department
As our new coordinator in Global Clinical Compliance you will be part of a well-functioning department, placed in Søborg. Together with 20 colleagues you will be responsible for ensuring that Novo Nordisk maintains one global clinical quality management system in compliance with GCP and other relevant external and internal requirements. The department is divided in two teams. The open position is located in the Clinical Support Team. The team consists of 9 dedicated colleagues, hereof seven GCP Advisors and two coordinators.

The Job
Together with the other coordinator you will be responsible for coordination of the internal quality assurance review process of all study protocols. The quality assurance review process involves coordinating a review of study protocols performed by a cross-functional council of dedicated experts for each clinical research activity. You will also be involved in other administrative tasks related to the team e.g. archiving and ad hoc administrative tasks.

Qualifications
Our new colleague must be quality-oriented, be able to handle many parallel activities at the same time, with different deadlines, and have a systematic approach. The ideal candidate has some practical experience in the clinical research field, e.g. as monitor, CTA, from laboratory work or similar. A high level of communication skills and a proficient level of spoken and written English are necessary. In-depth knowledge of the use of IT systems such as the Microsoft Office package is needed. Training in our specific IT systems will be provided.

You take a pragmatic approach to problem solving, and have strong interpersonal skills. You are organised and detail-oriented. You are a team player and thrive working across departments in an international organisation.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please contact Lisbeth Bonefeld +45 3075 8096 or Susanne Nørskov +45 3079 8151.

Deadline
22 April 2014.

Denmark - Søborg Administrative
04-Apr-2014 QA Engineer
Would you like to work in an international environment and be responsible for the quality assurance of components produced internally in Device Manufacturing Sourcing (DMS) on site Hillerød? Are you ready to ta...

QA Engineer

  • Quality
  • Denmark - Hillerød

Would you like to work in an international environment and be responsible for the quality assurance of components produced internally in Device Manufacturing Sourcing (DMS) on site Hillerød? Are you ready to take high impact decisions regarding the right level of quality to ensure patient safety? Then you might be the person we are looking for.

About the department
We are looking for a dedicated person with a high quality mind-set who will be part of the Manufacturing Quality Assurance team of 10 QA engineers. We are responsible for the quality assurance of all components produced internally in Novo Nordisk delivered for production of medical devices worldwide.

The job
As a QA engineer you will be responsible for ensuring and developing quality and compliance of the current production in DMS. You will make sure that our quality systems follow Novo Nordisk regulations, legal requirements, GMP, and ISO standards. You will review SOP documentation, write and approve change requests as well as approving non-conformity investigations. You will be part of a team with other experienced colleagues and have good opportunity for sparring. You will participate in investigations of root causes to non-conformities and customer complaints. In your daily work, you will interact with and be sparring partner for several departments such as Q-Support, Logistics, Quality Control, Mould and Pre-assembly production. You have direct access to the moulding and pre-assembly production and your success will depend on your ability to collaborate and communicate with all types of colleagues and business partners. Quality Mind-set and winning culture are incorporated concepts of our daily work.

Qualifications
First and foremost you have an excellent quality mind-set, good communication skills and you can place the importance of compliance on the agenda in a positive and constructive way.

You hold an academic degree and you preferably have 3-5 years of experience with quality assurance from the pharmaceutical, medical device or similar industry. It is an advantage if you have experience with ISO13485 or GMP, and Lean. Furthermore process insight in injection moulding and assembly production will be preferred.

Your language skills cover proficiency in English and Danish. You are known for finding constructive solutions as well as taking responsibility for your assignments. You enjoy the mixture of routine tasks and more challenging tasks, and you are flexible to changes in workload. Additionally, you work independently and you make decisions regarding quality tasks ensuring the right balance between quality demands, authority demands and business needs. You are structured and a team-player.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please call Lili Behjat Kristensen at +45 3079 4143.

Deadline
27 April 2014.

Denmark - Hillerød Quality
04-Apr-2014 Senior Programmer for Biostatistics Programming Anchor
Are you interested in working with biological data and would you like to be part of a future with a strong pipeline of products, which ensures huge variety of tasks, great opportunities for individual developme...

Senior Programmer for Biostatistics Programming Anchor

  • Research & Development
  • Denmark - Søborg

Are you interested in working with biological data and would you like to be part of a future with a strong pipeline of products, which ensures huge variety of tasks, great opportunities for individual development and influence on decision making?

Do you wish to work in a highly professional, engaged and global environment, where you can use your programming skills and quality mind-set bringing clinical projects to registration and market? You may be our new senior statistical programmer.

About the department
The Biostatistics Programming Anchor consists of 8 enthusiastic statistical programmers and process development specialists. The team is responsible for development and support of clinical data standardisation and reporting, planning and conduct of training within systems and processes, and maintenance and improvement of programming processes.

The team is part of Novo Nordisk’s large Biostatistics function with 150 statisticians and statistical programmers globally in our R&D clinical development organisation. Biostatistics is a dynamic department which cooperates with many different professionals in the organisation both within Denmark and across borders with our affiliates in the US, India, China and Japan, as well as our outsourcing partners in India. The job is situated in Copenhagen.

The job
As senior statistical programmer you will be involved in maintenance and development of SAS standard programs for reporting of clinical data. You will take part in system development and process improvement projects within statistical programming and you will give input to maintenance of global clinical data standards and data models Furthermore, you will be an active trainer and supporter in the global Biostatistics organisation.

You must take responsibility for both standard tasks and more complex and time critical tasks. Development of methods and processes, as well as knowledge sharing is continuously ongoing in Novo Nordisk, especially based on the initiative of the employees. Therefore we expect you to communicate programming/technical problems and ideas both internally and externally.

We expect you to take part in the maintenance of Biostatistics as a good and challenging place to work. In exchange we offer great opportunities for ongoing training to ensure the continued competency development of our employees.

Qualifications
You have a B.Sc. or M.Sc. within IT, natural sciences or other relevant degree, extensive knowledge and experience with SAS programming, IT system development methodologies, CDISC and clinical data domains. You have preferably five to eight years’ experience within clinical research and are able to write efficient, well documented and standardised computer programs. Furthermore, strong cooperation and analytical skills are a necessity. You are capable of working independently, take on responsibility and show initiative.

We expect you to be flexible and efficient. In addition we expect you to be able to overview several challenging tasks in parallel without compromising the quality of your work and that you remain high spirited, also when things are moving fast. Experience with project management and being a trainer will be an advantage.

Good collaboration and communication skills are necessary characteristics. You are also fluent in English.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please call Gert Bech Alding on + 45 3075 4892 or Tina Christiansen on + 45 3079 1748.

Deadline
27 April 2014.

Denmark - Søborg Research & Development
04-Apr-2014 Senior Programmer Biostatistics Copenhagen or Aalborg
Are you interested in working with biological data and would you like to be part of a future with a strong pipeline of products, which ensures huge variety of tasks, great opportunities for individual developme...

Senior Programmer Biostatistics Copenhagen or Aalborg

  • Research & Development
  • Denmark - Søborg

Are you interested in working with biological data and would you like to be part of a future with a strong pipeline of products, which ensures huge variety of tasks, great opportunities for individual development and influence on decision making?

Do you wish to work in a highly professional, engaged and global environment, where you can use your programming skills and quality mindset bringing clinical projects to registration and market? You may be one of our new statistical programmers.

About the department
The Biostatistics function is growing and consists currently of 150 statisticians and statistical programmers globally in our R&D clinical development organisation. Biostatistics is a dynamic department which cooperates with many different areas in the organisation both within Denmark and across borders with our affiliates in the US, India, China and Japan, as well as our outsourcing partners in India. Biostatistics provides a strong scientific community and we are organised in smaller units for each clinical project to ensure close collaboration with our various stakeholders.

The job
As senior statistical programmer your primary responsibility is to develop SAS programs based on clinical data for reporting of clinical trials, preparing summary documents and publications as well as supporting regulatory commitments. You handle many assignments concurrently and will work in close collaboration with a team of statisticians and statistical programmers.

You will be involved in coordinating and supervising the work of contract houses around the world performing outsourced programming tasks. Therefore we expect you to communicate programming/technical problems and ideas both internally and externally, as well as coach more junior colleagues. You must take responsibility for both standard tasks and more complex and time critical tasks.

Development of methods and processes, as well as knowledge sharing is continuously on-going in Novo Nordisk, especially based on the initiative of the employees. We expect you to take part in the maintenance of Biostatistics as a good and challenging place to work. In exchange we of course offer great opportunities for on-going training to ensure the continued competency development of our employees. The job can be situated in Søborg or in Aalborg.

Qualifications
You have a B.Sc. or M.Sc. within science, IT or other relevant degree, extensive knowledge and experience with the SAS programming language, as well as preferably experience within clinical research. You are able to write efficient, well documented and standardised computer programs. Furthermore, strong cooperation and analytical skills as well as an understanding for data structure are a necessity. You are capable of working independently, take on responsibility and show initiative.

We expect you to be independent and that you are flexible and efficient. In addition we expect you to be able to overview several challenging tasks in parallel without compromising the quality of your work and that you remain high spirited, also when things are moving fast. Experience with project management will be an advantage.

Good collaboration and communication skills are necessary characteristics. You are also fluent in English.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please call Birgitte Hylleberg Svendsen on + 45 3079 2510 or Malene Højbjerre on + 45 3079 6209.

Deadline
27 April 2014.

Denmark - Søborg Research & Development
03-Apr-2014 Clinical Trial Administrator
Would you like to join us in making a difference to people with diabetes? A job is waiting for you in a challenging and developing environment. ...

Clinical Trial Administrator

  • Administrative
  • Denmark - Søborg

Would you like to join us in making a difference to people with diabetes? A job is waiting for you in a challenging and developing environment.

About the department
Clinical Operations, Insulin and Devices-2 in Global Development is looking for a colleague to join us working as Clinical Trial Administrator. We have a team of experienced and enthusiastic International Trial Managers and Clinical Trial Administrators who are responsible for planning and conducting clinical trials within our fast acting insulin portfolio.

We offer a dynamic work place with dedicated colleagues who seek an atmosphere of trust and transparency.

The job
As Clinical Trial Administrator you will assist one or more International Trial Managers, who are responsible for conducting clinical trials. As Clinical Trial Administrator you will have a significant role in supporting the trial planning and execution by conducting trial related tasks.

Your main responsibility will be to manage the administrative tasks for the clinical team; take meeting minutes, help create presentations, coordinate website and newsletters, prepare and monitor clinical trial budgets, and establish and maintain trial master files. In addition you will be involved in the preparation and conduct of Monitor and Investigator meetings.

Qualifications
You have a BA in business administration or equivalent. You have 3-5 years of administrative experience from working in large and/or complex projects or line functions within the pharmaceutical industry. This will include experience with budgeting, accounting and project planning. You are proficient with both written and spoken English, and you have flair and interest for IT and technical solutions including the Microsoft Office Package.

Our ideal candidate has a structured approach to tasks, an analytical mind set and a proactive behaviour. Good communication skill, cross cultural understanding and ability to work in a complex and busy environment with a service minded attitude is a must.

At Novo Nordisk we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Contact
For further information, please contact Head of ClinOp, Insulin & Devices-2 Kirsten Bang Rungby +45 3079 6242.

Deadline
16 April 2014.

Denmark - Søborg Administrative
03-Apr-2014 Advanced System Analyst
Are you ready to make a difference for some of the most important IT systems in the NN R&D processes? The R&D Solution department supports a number of key projects in R&D, Global Development where N...

Advanced System Analyst

  • IT
  • Denmark - Bagsværd

Are you ready to make a difference for some of the most important IT systems in the NN R&D processes? The R&D Solution department supports a number of key projects in R&D, Global Development where NN’s clinical trials are planned and executed. If you are motivated by the opportunity to be part of a dedicated team with ambitions to continuously strive for state-of-the-art solutions together with the business, consider applying. R&D Solutions are looking for a new colleague to work in a group of 3 dedicated, highly skilled colleagues working on the CDW (Clinical Data Warehouse) & UNIX SCE (SAS analysis & reporting platform) Clinical systems.

About the department
R&D Solutions is part of IT system management under Corporate IT in Novo Nordisk A/S. You will be part of a highly engaged department of 12 employees responsible for managing the Novo Nordisk Clinical development applications. We manage the systems including, the support processes, new potential changes and the release lifecycle. Working closely with Global Development, we ensure their business processes are supported optimally by the IT systems. An open and honest dialogue is a core value and we set ambitious goals to which we are committed, as a team.

The Job
As an Advanced Business Analyst on the CDW & UNIX SCE platforms, you will be working to continuously develop and improve the functions these GxP systems provide to Global Development. Together with Line of Business you will help manage and develop superior technical solutions to be implemented on these systems. Close work with our vendor, challenging them on their technical solutions is a fundamental part of the job.

The preferred candidate would have a technical IT background, project management and application development skills, know GxP systems, Clinical Trial process, pharmaceutical compliance and system management. You must be able to work independently as you collaborate with different stakeholders in ITS, Global Development and vendors at both a global and virtual level. You will have ample opportunity for professional development and continuous improvement in your daily work.

Qualifications
You hold a Master’s degree in software engineering, computer science or a related technical discipline. You have 5+ years of project/system management experience with a proven track record of supporting and developing custom applications. An understanding of the following technologies, JAVA, SQL, PL/SQL, IBM DataStage, SAS and Unix would be beneficial, but, not required. We prefer if you are familiar with GxP impact systems and their validation requirements. You do not have to know the clinical trial systems, but, it will be an advantage. As a person you are dedicated to your tasks, a team player, have a good sense of humour and enjoy a busy, professional but also informal atmosphere.

You are fluent in both written and spoken English. Please submit your application online including motivational letter and CV in English.

In Novo Nordisk your skills, your commitment and your ambitions, will help us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.

Contact
For further information, please contact Christina Weber at +45 3075 2865.

Deadline
20 April 2014

Denmark - Bagsværd IT
02-Apr-2014 Internship in FLIR Consulting
Novo Nordisk is one of the world’s most successful pharmaceutical companies. At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join...

Internship in FLIR Consulting

  • Student and Internships
  • Denmark - Bagsværd

Novo Nordisk is one of the world’s most successful pharmaceutical companies. At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort.

FLIR Consulting (Finance, Legal, Investor Relations) is an internal consultancy reporting to our CFO. We support the organisation by driving a number of key strategic projects throughout Novo Nordisk’s global operations.

Our internships provide exciting learning opportunities for master’s degree students who bring new ways of thinking to our company.

About the department
You will be part of a young, diverse department consisting of 12 dedicated employees with backgrounds from top-tier consultancies (e.g. McKinsey & Co, Bain & Co, etc.) or with previous Novo Nordisk experience.

The internship offers your first-hand experience of working with some of the best strategy consultants, and will provide you a steep learning curve with exposure to best practice project management methods and tools.

The job
As an intern in FLIR Consulting, you will participate in various projects as a junior consultant together with more experienced project members. Your tasks will vary widely, and include analyses, information gathering, participating in team problem solving, and independently driving own work streams.

Qualifications
You are among the best in your class and take an interest in consulting, corporate finance and project management. You are a master’s degree student in Economics, Business Administration, Engineering or similar in the first or second year of your studies. You are fluent in English, and are used to both working independently and in teams. Finally, you have excellent problem solving skills and a positive attitude.

Your development is important to us. Training and personal development are key tools to ensure continuing development of your toolbox.

Practicalities:

Period: The internship position is a full-time position for 5-6 months

Start date: 1 August 2014

Contact
For further information, please call Nina Correll on + 45 3075 5009.

Deadline
1 May 2014.

Denmark - Bagsværd Student and Internships
02-Apr-2014 International Trial Manager
In this job, 300.000 people worldwide depend on you to develop the world’s best bleeding disorder treatments. If you find challenges like this exciting and inspiring, you may be our new International Trial Mana...

International Trial Manager

  • Research & Development, Trial Manager
  • Denmark - Søborg

In this job, 300.000 people worldwide depend on you to develop the world’s best bleeding disorder treatments. If you find challenges like this exciting and inspiring, you may be our new International Trial Manager within our Haemophilia project portfolio.

About the Department
Haemophilia, Clinical Operations is a team of 70 highly skilled and ambitious colleagues responsible for planning and execution of clinical trial activities in accordance with the Clinical Development Plans within haemophilia and rare bleeding disorders. The scope of our activities is phase 1 to 4 clinical trials in collaboration with our Novo Nordisk affiliates and Contract Research Organisations. Our environment is characterised by a vast global network with interesting assignments, flexible working conditions, continuous personal and professional development and exciting opportunities which come when working for a large headquarter function.

The job
As International Trial Manager you will be responsible for timely planning, executing and finalizing clinical trials using your operational and therapeutic experience. You will coordinate trial management activities in a proactive fashion through clear communication and good team work. As a chairperson of the international study team you will organise and execute team meetings and ensure the involvement of relevant stakeholders for decision making. You will participate in and contribute to relevant Investigators and Monitor meetings. You have a structured and analytical approach during development of critical trial documents like the trial protocol, and at the same time you have an eye for important details while keeping the overview. You are able to digest complex data output and to evaluate the adequate levels of quality in all you do. By joining us you will get the opportunity to further develop your competencies within trial management in an international environment.

Qualifications
You hold a university degree in medical, biological, pharmaceutical science or equivalent with at least 2 years of experience in trial management related positions. You have a broad knowledge of clinical trial methodology and you have good presentation, communication and negotiation skills. A quality mind set is a must, together with a focus on meeting deadlines, communicating effectively and knowing how to prioritise between different tasks in a dynamic environment. You are a dedicated team player with a high degree of flexibility and cross-cultural awareness who inspires trust amongst colleagues and partners. Fluency in written and spoken English is essential. Experience in running non-interventional studies is of advantage, as well as knowledge of life cycle management.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please Contact Karolina Rask on +45 3079 2670 or Nis Hjortskov Jensen on + 45 3079 7857.

Deadline
21 April 2014.

Denmark - Søborg Research & Development, Trial Manager
02-Apr-2014 PostDoc Fellow for a Pharmacoepidemiologic Research Project
Novo Nordisk is participating in the European GetReal project, under the Innovative Medicines Initiative (IMI). IMI is Europe's largest public-private research program aimed at optimizing the development of bet...

PostDoc Fellow for a Pharmacoepidemiologic Research Project

  • Research & Development
  • Denmark - Mørkhøj/Søborg

Novo Nordisk is participating in the European GetReal project, under the Innovative Medicines Initiative (IMI). IMI is Europe's largest public-private research program aimed at optimizing the development of better and safer medicines for patients (http://www.imi.europa.eu).

We are looking for a PostDoc fellow to join the Health Economics & HTA department and work on the GetReal project for a 12 months period with possibility for extension.

About the department
The Health Economics & HTA department is part of Global Development, caretaking all clinical development projects in Novo Nordisk. Health Economics & HTA is responsible for health economic input to project in the Novo Nordisk’s R&D pipeline and the department consists of 12 experienced health economists with a diverse background. You will report to the Director of Health Economics and HTA and work closely with the project lead for the GetReal project. The department is responsible for generating evidence that support the value of the Novo Nordisk development products. You will have cross-functional interactions with multiple stakeholders in Novo Nordisk, including Regulatory Affairs, Epidemiology, and other PhD/PostDoc fellows. External stakeholders and partners will be universities, health authorities and other members of the IMI project. Travels will be expected as this is an international collaboration.

The job
The overall objectives of GetReal are (1) for pharmaceutical R&D and healthcare decision makers to better understand how real-world data and analytical techniques can be used to improve the relevance of knowledge generated during development, e.g., through innovation in clinical trial design, and (2) to develop tools to better predict the effectiveness of a drug, before launch. Designs of studies with electronic health care databases and pragmatic trials will be proposed. Furthermore you will be looking at how to deal with a more flexible experimental design: dynamic exposure, adaptive designs, etc.

The work is related to one of the work packages of the GetReal project and includes collaboration with universities in the Netherlands and in the United Kingdom. The specific work package aims at identifying key drivers of effectiveness to understand why and to which extent efficacy differs from effectiveness and to provide tools to address this gap. The postdoc will work on how more “pragmatic” clinical trials before launch can be performed and analyse electronic health care databases, do literature reviews as well as looking at pragmatic trial designs.

You will be responsible for collaboration between Novo Nordisk and the universities in the work package. You will ensure that the work is in line with the scope of the project, from an R&D perspective.

You will fully participate in the elaboration of the protocols for pilot studies, the execution of the pilot studies and the publication of studies.

Qualifications
You have a PhD degree from Public Health sciences, epidemiology, pharmaco-epidemiology or Health Economics and advanced knowledge about statistical methods.

On the personal side, strong communication skills and analytical skills are needed, as well as a proven ability to work independently and efficiently with various external and internal stakeholders.

Practicalities

Period: The position is a full-time position for 1 year. The project runs until end of 2016, and it will be possible to extend if expectations on both sides are met.

Start date: 01 May 2014 or later.

Contact
For further information, please call Mark Aagren on + 45 30799976 or Erpur Adalsteinsson on + 45 30751737.

Deadline
25 April 2014.

Denmark - Mørkhøj/Søborg Research & Development
01-Apr-2014 Document and system responsible
Would you like being responsible for assuring the quality of the Document and Record Management process in Novo Nordisk A/S Device Manufacturing Development? And are you highly motivated by stakeholder manageme...

Document and system responsible

  • Quality
  • Denmark - Hillerød

Would you like being responsible for assuring the quality of the Document and Record Management process in Novo Nordisk A/S Device Manufacturing Development? And are you highly motivated by stakeholder management. Then you might be the right person for the job as Document and Record Manager in Device Manufacturing Development (DMD).

About the department
You will be part of a team of 13 dedicated colleagues in Hillerød. Together, we are responsible for the Quality Management System in DMD. We are the local documentation centre, we have core process experts in Change Control and Non Conformity handling and many other Quality Systems responsibilities. We are also responsible for assuring the quality of Quality Control, manufacturing processes and laboratories for Novo Nordisk newest developed Medical Devices and make them ready for pilot production and low volume production for clinical trials and launch to the market. The team values professional sparring and you can look forward to entering into an energetic and positive working environment where cooperation is a keyword.

The job
You will be an important part of developing our record management system in our area of Novo Nordisk A/S and maintaining the record and document system. You will be the one in our area who advise and help our users of the document and record management process flow and how to use the IT system and tools. You will handle daily operations in our local Documentation Centre. By engaged and focused commitment you ensure all tasks solved and KPI’s fulfilled timely as well as commitment in the team to ensure high level of team spirit.

Learn more about Novo Nordisk Product Supply and working in QA using this link www.novonordisk.com/careers/QA

Qualifications
You hold a bachelor degree e.g. librarian. Preferably you have experience within the pharmaceutical or Medical Device industry. Furthermore, you have a minimum of 3 years work experience from archives, library, record- and document management. You are outgoing, have a strong quality mind-set. Moreover, you have a high level of fluency in written and spoken English.

On a personal level, you are known for dedicating yourself to working proactively to solve the task at hand. Using your ability to think out of the box, you are still able to come up with solutions or suggestions that comply with quality requirements. You are a team player and a skilled communicator, and you thrive on unfolding your high level of energy and spirit in an international, dynamic environment.

Feel free to submit your job application in either English or Danish, whichever you prefer. Applications are reviewed on a rolling basis so please apply as soon as possible.

At Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.

Contact
For further information, please call Dean Kloe on + 45 3075 8948.

Deadline
21 April 2014.

Denmark - Hillerød Quality
01-Apr-2014 Category Management
Do you have a strong business mind-set and are you looking for a job with the possibility to further develop your skills and competences within category management, market and spend analysis, stakeholder manage...

Category Management

  • Sourcing
  • Denmark - Bagsværd

Do you have a strong business mind-set and are you looking for a job with the possibility to further develop your skills and competences within category management, market and spend analysis, stakeholder management, negotiations and contracting.

About the department
Corporate Procurement is, in close cooperation with affiliates and stakeholders, responsible for purchasing, sourcing and contracting of the global indirect spend in Novo Nordisk. Corporate Procurement has more than 100 employees and is anchored in the Corporate Finance organisation. You will be part of a dynamic and enthusiastic group of 6 team members in the Marketing Services team. We are part of Marketing, Professional & Travel Management Services Department and hold the responsibility for the marketing related service categories.

The Job
As Associate Category Manager you will have a variety of operational sourcing tasks and act as commercial anchor-point between our suppliers and our organisation. Amongst others the tasks include: support creation of a sourcing pipeline of upcoming marketing projects, conducting structured tender processes in accordance with the standard Novo Nordisk sourcing model, support on contract negotiations and compliance related tasks and establishing strong stakeholder relationships across our global organisation. On larger projects you will team up with senior colleagues to support you professionally and to drive your personal development.

You will also be involved in the establishment and implementation of category strategies including: business and market intelligence facilitating fact-based decision making, incl. development of cost models, excellent supplier relationship management and ensuring value creation for different business areas across Novo Nordisk in line with category strategies.

Qualifications
The ideal candidate has 2-5 years working experience. We expect you to have a relevant Master degree with excellent results and a track record of strategic sourcing of professional services – preferably within marketing related services. You possess a combination of project management and strong analytic capabilities, together with excellent people skills and lots of humour. You are able to advise senior stakeholders on best sourcing practices as well as on commercial aspects during negotiations. The ideal candidate has experience from or interest in negotiation of both specific delivery contracts and frame agreements

As a person you are ambitious and a proactive self-starter driven by achieving the best possible results while acting in a responsible and ethical way. You are a well-liked colleague and a team player. You easily establish a high level of trust and commitment with colleagues, stakeholders and suppliers. Your ability to connect and relate to internal stakeholders is a key competency, and a proven track record from a larger organization is an advantage.

You master English fluently, both written and spoken.

In Novo Nordisk, your skills, your dedication and your ambition help us improve many people’s lives. In exchange, we offer you an opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.

Contact
For further information, please contact Morten Bøgh Skaarup at +45 3075 3618.

Application:Please send your application in English via Novo Nordisk website (www.novonordisk.com) and mark the application with no. 21162BR Associate Category Manager

Deadline
30 April 2014

Denmark - Bagsværd Sourcing
01-Apr-2014 Category Manager
Do you have a strong business mind-set and are you looking for a job with the possibility to further develop your skills and competences within category management, market and spend analysis, stakeholder manage...

Category Manager

  • Sourcing
  • Denmark - Bagsværd

Do you have a strong business mind-set and are you looking for a job with the possibility to further develop your skills and competences within category management, market and spend analysis, stakeholder management, negotiations and contracting.

About the department
Corporate Procurement is, in close cooperation with affiliates and stakeholders, responsible for purchasing, sourcing and contracting of the global indirect spend in Novo Nordisk. Corporate Procurement has more than 100 employees and is anchored in the Corporate Finance organisation. You will be part of a dynamic and enthusiastic group of 6 team members in the Marketing Services team. We are part of Marketing, Professional & Travel Management Services Department and hold the responsibility for the marketing related service categories.

The Job
As Category Manager you will drive the establishment, implementation and maintenance of allocated category strategies including: business and market intelligence facilitating fact-based decision making, incl. development of cost models, excellent supplier relationship management and ensuring value creation for different business areas across Novo Nordisk in line with category strategies.

You will also lead a variety of operational sourcing tasks and act as commercial anchor-point between our suppliers and our organisation. Amongst others the tasks include: creation and ownership of a sourcing pipeline of upcoming marketing projects, leading a structured tender processes in accordance with the standard Novo Nordisk sourcing model and on larger projects guide and support junior colleagues, driving contract negotiations and ownership of compliance related tasks and establishing strong stakeholder relationships across our global organisation.

Qualifications
The ideal candidate has at least 5-8 years working experience. We expect you to have a relevant Master degree with excellent results and a solid track record of strategic sourcing of professional services - preferably within marketing related services. You possess a combination of project management and strong analytic capabilities, together with excellent people skills and lots of humour. You are able to advise senior stakeholders on best sourcing practices as well as on commercial aspects during negotiations. You are also experienced in commercial negotiations of both specific delivery contracts and frame agreements.

As a person you are ambitious and a proactive self-starter driven by achieving the best possible results while acting in a responsible and ethical way. You are a well-liked colleague and a team player. You easily establish a high level of trust and commitment with colleagues, stakeholders and suppliers. Your ability to connect and relate to internal stakeholders is a key competency, and a proven track record from a larger organization is an advantage. You master English fluently, both written and spoken.

In Novo Nordisk, your skills, your dedication and your ambition help us improve many people’s lives. In exchange, we offer you an opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.

Contact
For further information, please contact Morten Bøgh Skaarup at +45 3075 3618.

Application: Please send your application in English via Novo Nordisk website (www.novonordisk.com) and mark the application with no. 20805BR Category Manager

Deadline
30 April 2014

Denmark - Bagsværd Sourcing
01-Apr-2014 QMS Coordinator
This is your chance to use your knowledge about GMP and Quality systems to help the Research & Development Engineers bring forward game changing devices. ...

QMS Coordinator

  • Quality
  • Denmark - Hillerød

This is your chance to use your knowledge about GMP and Quality systems to help the Research & Development Engineers bring forward game changing devices.

About the department
We are a six month old department and it is our responsibility that quality system is up to date with the Novo Nordisk systems and regulations and that research and development is done in compliance. You will be responsible for administration and development of key elements of the quality system and be in contact with the entire organisation.

The Job
You will refer to the Quality VP and work with an experienced QMS coordinator. You will be responsible for administration, review and filing of non-conformities, change requests and CAPAs. You will be site responsible for the Quality Activity system. You will be involved in audit and inspections during planning, execution and follow up.

You will be backup super user in our training system. You will make trend reports to management.

Qualifications
You have experience with Quality management in medical devices or pharmaceuticals from previous jobs and have a technical background. You are well organised and it is easy for you to make sure that systems and documentation are always ready to be inspected. You motivate colleagues to follow the systems and follow up systematically. You work effectively in databases. You have a good understanding of data that you use to produce high quality reports. You speak and write English fluently.

In Novo Nordisk it will be your skills engagement and ambitions that will help us develop the devices that improve the daily lives of patients worldwide. We offer you a workplace with skilled colleagues and possibility for professional and personal development

Contact
For further information, please call Mirela Vrzogic at +45 3075 1471.

Deadline
21 April 2014

Denmark - Hillerød Quality
31-Mar-2014 Talented MD with ambitions to work in the pharmaceutical industry
We are looking to employ one or more talented Medical Doctor(s) with passion for science and clinical research and an interest to initiate a career in the pharmaceutical industry. Join us and you’ll be working ...

Talented MD with ambitions to work in the pharmaceutical industry

  • Research & Development, Medical Doctor
  • Denmark - Søborg

We are looking to employ one or more talented Medical Doctor(s) with passion for science and clinical research and an interest to initiate a career in the pharmaceutical industry. Join us and you’ll be working with highly talented colleagues, every one of whom strives passionately to create better treatments and care. We offer flexibility and the possibility to be part of an inspiring environment, where there is room for personal development and an increased insight into the medical areas of diabetes and obesity.

About the department
Liraglutide & Obesity Medical & Science is a department comprised of sub-teams of medical specialists, who are working with GLP1 agonists being developed for treatment of diabetes and obesity. Our main tasks include the responsibility for the clinical development programmes, design of new clinical studies, collaboration with clinical operational staff and investigators and scientific experts in obtaining new groundbreaking data. Finally interpreting and concluding on the data obtained in our clinical trials and supporting communication of these data at scientific meetings or to regulatory authorities are also a main part of our tasks.

Our organisation is project-centric and internally we work in cross-functional teams typically including project managers, medical marketing, statistics, clinical operations and medical writers. Our key external stakeholders are the scientific community and medical experts, regulatory authorities and market access institutions.

The medical and science department is part of Global Development located in Søborg.

We take pride in the many patients our work affects.

The job
As an International Medical Manager, you will take on a broad role, where focus and daily tasks vary to a great extent, depending on the assigned project and study life cycle stage. It will include working with your medical colleagues in supporting interpretation and documentation of clinical data potentially leading to new drug applications (NDA’s) or variation applications. Introduction to clinical trial design and writing of study protocols will also give you an important possibility to develop your skills in the drug development area. Finally, supporting the medical assessment of safety data with our drugs in clinical development can become your responsibility. Naturally, you will also need to keep yourself updated on medical literature and participate in congresses as part of the job.

The job is globally oriented and will require collaboration with highly skilled colleagues from other areas and external stakeholders including regulatory bodies, treating physicians and therapeutic experts, hence you may expect travelling activity of approximately 10%.

Qualifications
You must hold a university degree as a Medical Doctor. Moreover, you must have passed post-graduate internship and thereafter you have done 2-5 years of clinical practice. We strongly prefer that you have documented research experience, most likely from a Ph.D. within an area related to diabetes/endocrinology or obesity. Of course, we welcome that you have experience from executing clinical trials and/or interaction with health authorities, but most importantly you have the interest and passion to learn.

You are a flexible, open-minded and dedicated team player, who thrives in a global environment of continuous development, and focuses on high quality and results. You have a good sense of humour and value working in a team. We put patients first and do not compromise on quality and expect you to do the same. Interaction with internal and external global experts require proficiency in English, excellent communication, coordination and planning capacities.

We offer an inspiring and ambitious working environment, alongside the flexibility that allows you to shape your own working day. We believe that’s what stimulates the ingenuity to develop the next generations of cutting-edge treatments.

Contact
For further information, please contact Director, 4177 Medical & Science, Liraglutide & Obesity, Anne Bloch Thomsen at +45 3079 0289.

Deadline
4 May 2014

Denmark - Søborg Research & Development, Medical Doctor
31-Mar-2014 Experienced MD with interest in clinical research and drug development
We are looking to employ one or more experienced Medical Doctor(s) with passion for clinical research and development to help us develop new and improved treatments to people who need them. Join us and you’ll b...

Experienced MD with interest in clinical research and drug development

  • Research & Development, Medical Doctor
  • Denmark - Søborg

We are looking to employ one or more experienced Medical Doctor(s) with passion for clinical research and development to help us develop new and improved treatments to people who need them. Join us and you’ll be working with highly talented colleagues, every one of whom strives passionately to create better treatments and care. We offer the opportunity to go in-depth with clinical challenges and the most recent frontline scientific discoveries within the areas of medical treatment of obesity or type 1 and type 2 diabetes. We work in a dedicated but flexible environment and we would like you to share our efforts in doing the utmost to improve our patients’ lives.

About the department
Liraglutide & Obesity Medical & Science is a department comprised of sub-teams of medical specialists, who are working with GLP1 agonists being developed for treatment of diabetes and obesity. Our main tasks include the responsibility for the clinical development programmes, design of new clinical studies, collaboration with clinical operational staff and investigators and scientific experts in obtaining new groundbreaking data. Finally interpreting and concluding on the data obtained in our clinical trials and supporting communication of these data at scientific meetings or to regulatory authorities are also a main part of our tasks.

Our organisation is project-centric and internally we work in cross-functional teams typically including project managers, medical marketing, statistics, clinical operations and medical writers. Our key external stakeholders are the scientific community and medical experts, regulatory authorities and market access institutions.

The medical and science department is part of Global Development located in Søborg. We take pride in the many patients our work affects.

The job
As an International Medical Director, you will take on a broad role, where focus and daily tasks vary to a great extent, depending on the assigned project and study life cycle stage. We can offer participation in projects across several stages of the clinical development cascade.

We expect that you are capable of taking on the responsibility of being the medical lead in either early or late stage clinical development projects, collaborate closely with your team colleagues and the project vice president. Your area of responsibility will be to provide the medical expertise within the area of diabetes or obesity and to ensure relevant progression and decision making to the clinical development process while ensuring adequate stakeholder management.

Your tasks could also include being instrumental in providing medical and scientific support to interpretation and documentation of clinical data leading to new drug applications (NDA’s) or variation applications, as well as regular safety updates on marketed drugs and drugs in clinical development.

You will collaborate closely with a variety of colleagues across the Novo Nordisk organisation and across skill areas. The job is globally oriented and may include some travel activity of approximately 10% of your time.

Qualifications
You must hold a university degree as a Medical Doctor and most likely you also hold a Ph.D. within an area related to our research. Either you are an experienced specialist within obesity or diabetes or you have relevant experience with clinical development from the pharmaceutical or biotech industry. This may ideally include experience in executing clinical trials and interaction with health authorities. Most importantly you have a passion for clinical development.

You are a flexible, open-minded and dedicated team player with the ability to take on a team lead role and share your expertise with the team. In addition, you thrive in a global environment of continuous development, and focus on high quality and scientific results.

We put patients first and do not compromise on quality and expect you to do the same. Interaction with internal and external global experts require proficiency in English, excellent communication, coordination and planning capacities.

We offer an inspiring and ambitious working environment, alongside the flexibility that allows you to shape your own working day. We believe that’s what stimulates the ingenuity to develop the next generations of cutting-edge treatments.

Contact
For further information, please contact Director, 4177 Medical & Science, Liraglutide & Obesity, Anne Bloch Thomsen at +45 3079 0289.

Deadline
4 May 2014

Denmark - Søborg Research & Development, Medical Doctor
28-Mar-2014 Medical Writing Specialist
Clinical Reporting is looking for medical writing specialists. You will be offered a challenging job with a significant amount of individual responsibility, and good personal development opportunities in an int...

Medical Writing Specialist

  • Research & Development
  • Denmark - Søborg

Clinical Reporting is looking for medical writing specialists. You will be offered a challenging job with a significant amount of individual responsibility, and good personal development opportunities in an international and dynamic atmosphere.

About the department
Clinical Reporting is the medical writing function at Novo Nordisk and is part of Global Development. We are currently 60+ employees, primarily medical writers and clinical publishers. We are a diverse group with different nationalities and professional backgrounds working together in a pleasant and informal atmosphere. We are responsible for preparing clinical documents for submission to regulatory authorities worldwide as well as abstracts and posters for scientific conferences and manuscripts to scientific journals.

The job
As medical writing specialist, your main tasks involve preparation of complex clinical documents within Novo Nordisk’s different therapy areas. Planning and coordination of activities in a cross-disciplinary setting is a central part of the job. Your main collaboration partners include clinicians, statisticians, regulatory affairs professionals, trial managers and data managers from Novo Nordisk headquarters and international affiliates.

Another important component of the job is mentoring and training of other medical writers, which requires the ability to provide constructive feedback. The medical writing specialist is also expected to drive sharing of better practices across projects/processes.

All documents are written in English and must comply with internal Novo Nordisk standard operating procedures as well as external guidelines.

Qualifications
You have a university degree within natural sciences (MD, M.Sc., M.Sc.Pharm. or equivalent) and ≥5 years of medical writing experience. In addition, you have a good understanding of the pharmaceutical industry, including clinical development and regulatory processes and requirements. Your professional skills also include statistics and scientific research methods, and you have experience with writing publications for scientific journals. You master written and spoken English at a professional level, and you have a flair for, and a genuine interest in scientific communication. In addition, you should be able to communicate in a reliable, professional and trustworthy manner. You are a strong team player who adapts easily to a changing environment with tight deadlines, and you are good at planning, coordinating, managing stakeholders and reaching consensus. You are thorough, structured and conscientious, and you have a good sense of humour.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous development.

Contact
For further information, please call Ann Olling +45 3079 7294 or Tine Møller +45 3075 7052.

Deadline
20 April 2014.

Denmark - Søborg Research & Development
28-Mar-2014 Quality Engineer
Would you like to help securing Novo Nordisk A/S portfolio of durable devices continuously is improved to the benefit of our customers? Do you get energised by working in a team; handle multiple tasks on a dail...

Quality Engineer

  • Quality
  • Denmark - Hillerød

Would you like to help securing Novo Nordisk A/S portfolio of durable devices continuously is improved to the benefit of our customers? Do you get energised by working in a team; handle multiple tasks on a daily basis in a global environment? Then you might be the person we are looking for in Device Manufacturing Development (DMD), Durable QA.

About the department
DMD Durable QA is responsible for quality assurance activities and continuous optimization of the Novo Nordisk A/S portfolio of durable devices. The department works with suppliers and assembly sites that are located in Denmark, Europe and China. Your closest colleagues are 50 highly qualified professionals within Device Manufacturing Development (12 of these in Durable QA) working with the QA support to both marketed and new products within the durable device area. The working relations are informal and the team values professional sparring and good humour highly.

The job
You will contribute to the Device Manufacturing Development organisation by representing Quality Assurance. That is: Continuous improvement of the Quality Management System for durable devices, ensuring the right product quality and supporting the alignment of quality ambitions across the entire supply chain. The responsibility of the department also includes support to costumer complaint investigation, QA support to optimization projects and documentation of changes to both product and processes, support to incident handling when requested from the Manufacturing sites and building strong partnerships with internal stakeholders within Manufacturing, Device R&D and Manufacturing Development.

You will be QA responsible for a number of durable components and represent QA in the continuous improvement projects. You will prepare and maintain the quality component specifications, ensure that the quality of the components is according to the specified criteria’s. You will also be QA reviewer on change requests and non-conformities related to the components.

In your daily work, you will interact with several departments internally and externally and your success will depend on your ability to be a role model with regards to collaboration and communication with all types of colleagues and business partners.

The position offers you a unique opportunity to leave your mark on the department while realising your goals and seeing the benefits of your work. Overall, you will have a great degree of freedom in the job working with long-term deadlines that give you the opportunity to plan your own day-to-day work.

When you start you will undergo an individual and intense training program.

Qualifications
You hold a relevant academic degree in engineering, pharmacy or equivalent with 3-5 years of experience. Preferable your academic background is topped with experience with injection moulding processes and you are experienced in understanding mechanical drawings. However we would also like to hear from talented newly academic graduates.

You have an excellent quality mindset, good communicational skills and you can place the importance of compliance on the agenda in a positive and constructive way.

Your language skills cover proficiency in English, and it is an advantage if you have experience with production and/or quality assurance within the pharmaceutical industry. It is also an advantage if you have knowledge with the requirements ISO 13485, 21 CFR Part 820 and ISO 14971.

As a person, you are known for a high commitment to finding constructive solutions as well as taking responsibility for your assignments.

You work independently and make decisions regarding quality tasks and ensure the right balance between quality demands, authority demands and business needs. At the same time, you perform well in a team-oriented environment.

In Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.

Contact
For further information, please contact Malene Fugl Andersen on + 45 3075 8982.

Deadline
17 April 2014.

Denmark - Hillerød Quality
28-Mar-2014 Chemist
Are you ready to make a difference? And are you committed to support a GMP production in Novo Nordisk? Then you might be our new chemist. We are looking for a production chemist with a high quality mindset and ...

Chemist

  • Production
  • Denmark - Gentofte

Are you ready to make a difference? And are you committed to support a GMP production in Novo Nordisk? Then you might be our new chemist. We are looking for a production chemist with a high quality mindset and GMP experience to join us in the glucagon filling production, a part of Biopharm Aseptic Production.

About the department
The job is located in the department producing glucagon vials. We are responsible for the following process steps: formulation, filling (in isolators), freeze drying, capping & inspection. There are 110 employees in the department, located in Gentofte, Denmark. The open position is in the Process Team, where you will work with 8 highly engaged colleagues.

The Job
In close collaboration with your colleagues in the process team, you will ensure that the filling processes are in compliance with all regulations. You will support the operators in the daily production and secure that we live up to the requirements of our quality management system. As such you will spend time on the shop-floor, knowing that being close to the process and the operators will help you solving problems early and effectively.

On an on-going basis, you will handle systematic problem solving, non-conformities, validations and batch documentation. Additionally you will optimise the production processes in close collaboration with other support functions and the QA-functions. You will also drive compliance improvement projects. As you will be part of the production support team you will be expected from time to time to support production on doing trouble shooting also outside normal working hours. You can expect a dynamic and varied working day with an informal atmosphere and good colleagues.

Our department is highly motivated and this position offers you a unique opportunity to strengthen your experience in a GMP production environment, realise personal as well as department goals and see the benefits of your work. This position is classified in the highest category for professionals. You will experience an enthusiastic working atmosphere where we take a personal responsibility for quality, delivery and each other.

Qualifications
You hold a MSc in Engineering or Pharmacy with minimum 3 years of relevant experience within pharmaceutical production. You have a strong mind-set for quality and compliance and like to spend time in the production. As a person you can stay focused in a busy working day and you always approach tasks and colleagues with a positive attitude and energy. You are analytical and work in a structured way and you are used to deliver according to deadlines. You are fluent in both English and Danish.

At Novo Nordisk, your skills, dedication and ambition help us to change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please contact Sara Belhiba on + 45 3075 5141.

Deadline
28 April 2014.

Denmark - Gentofte Production
28-Mar-2014 Vice President
Are you passionate about Quality and making a difference for your stakeholders? Do you want influence and are you ready to impact decisions? And are you motivated by developing your team and your employees? If...

Vice President

  • Quality, senior position
  • Denmark - Bagsværd

Are you passionate about Quality and making a difference for your stakeholders? Do you want influence and are you ready to impact decisions? And are you motivated by developing your team and your employees?

If you can answer ‘yes’ to the above, you could be our new leader of Quality Affiliates and Marketing.

About the department
Quality Affiliates and Marketing (QAM) is a team in Corporate Quality who provides quality and compliance support to Novo Nordisk Affiliates and Regions as well as Marketing & Medical Affairs. Moreover, QAM is the voice of the Affiliates, Regions and Marketing in various headquarter forums and projects.

The Vice President of QAM reports to the head of Corporate Quality, Executive Vice President Lars Fruergaard Jørgensen, and is a member of the Corporate Quality Management team and the Novo Nordisk Quality Management team. The department is based in headquarters in Copenhagen.

Further, the Vice President of QAM also takes on the role as the Quality partner towards Operations Management, headed by President and COO Kåre Schultz.

The Job
In headquarters, you will be the leader of a small team of specialists, and responsible for continuous development of the team’s specialist knowledge and deliverables; and for creating an engaging work environment that motivates and develops your people.

At a global level, you will be responsible for leading a cross-organisational management team with Quality leaders from the regions and Marketing & Medical Affairs; and you will set direction in alignment with your stakeholders’ priorities.

The job offers a unique opportunity to meet and interact with stakeholders at all levels of the organisation and from around the globe. With the global reach of the position, travel is an integral part of the job.

Qualifications
You have an academic background – preferably within e.g. pharmacy, chemistry, biology or engineering. You have a deep insight into quality and a profound knowledge and understanding of quality management systems. You act with integrity and can make challenging decisions, balancing compliance and business requirements.

You are a strong and experienced leader and you have a proven track record of excellent communication and stakeholder management.

Furthermore, significant international experience from a sales and marketing unit and cultural awareness are crucial to succeed in this position.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please call Lars Fruergaard Jørgensen on +45 3079 8551 or Charlotte Devantié Olesen on +45 3079 7234.

Deadline
21 April 2014.

Denmark - Bagsværd Quality, senior position
26-Mar-2014 QA Chemist
Do you want to be part of Quality Assurance and ensure a high level of quality of Novo Nordisk’s insulin products and hereby make a difference for thousands of people? Quality Assurance in Hilleroed is looking ...

QA Chemist

  • Quality
  • Denmark - Hillerød

Do you want to be part of Quality Assurance and ensure a high level of quality of Novo Nordisk’s insulin products and hereby make a difference for thousands of people? Quality Assurance in Hilleroed is looking for a talented and ambitious QA chemist to help assure the quality of the laboratories in the Danish part of the production of insulin.

About the department
The new position is an expansion of the team and we are expanding due to increasing demands related to laboratories in the pharmaceutical industry. We are looking for a QA chemist for approval of documentation from both the chemical laboratory in Hilleroed and the microbiological laboratory in Bagsvaerd. You will join a dynamic department of 39 dedicated employees, divided into three teams, all working with the quality assurance of our insulin products. You will become part of an ambitious team with an informal relation, good humour and where we take care of each other. In that way you will rapidly, as a new employee, become a part of the team. In our department we are open and honest and appreciate a colleague which takes responsibility and have a positive approach to new challenges.

The Job
As a QA chemist you will be involved in and be responsible for activities, which are necessary ensure a high level of compliance in the chemical- and microbiological laboratory.

In addition to approval of documentations related to the laboratories, such as laboratory investigations, deviations and change request, you will be involved in handling of quality issues, where we use the LEAN tools to ensure that we systematically have solved our problems. QA is an important player at internal audits and external authority inspections, where you are expected to participate and present data when needed.

Being a new member of the team, you will undergo a structured and individual training program with your colleagues acting as the trainer, and you can expect increasingly more responsibility. Subsequently, you will have an individual development plan to ensure continuous development and realization of your potential.

You can read more about working in QA by visiting the following link: www.novonordisk.com/careers/QA

Qualifications
You hold an academic degree, e.g. pharmacist, veterinarian, biochemist, or similar. You have a quality mind-set, meet your deadlines and with your structured approach to your tasks you stay organized - even in a changing and busy environment where priorities can quickly change.

You welcome changes and challenge usually our way of doing things so we will be even better. Finally, you can communicate in both Danish and English written as well as spoken.

In Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve the lives of people with diabetes. In return we offer you the opportunity to work with talented colleagues, and in addition to that we offer you opportunities for professional and personal development.

Contact
For further information about the position, please contact Morten Petersen on +45 3075 0663.

Deadline
16 April 2014.

Denmark - Hillerød Quality
26-Mar-2014 Medical Specialist
In this job you will be working in Medical & Science, Insulin & Devices. The department aim is to provide maximal value to our development drug and device portfolio and marketed products through medical...

Medical Specialist

  • Research & Development, Medical Doctor
  • Denmark - Søborg

In this job you will be working in Medical & Science, Insulin & Devices. The department aim is to provide maximal value to our development drug and device portfolio and marketed products through medical, clinical, and scientific excellence and innovation. If you find it challenging and inspiring to be part of an international team of specialists, you might be our new Medical Doctor within diabetes drug and device development.

About the department
Medical & Science, Insulin and Devices at Novo Nordisk A/S headquarter is looking for a medical doctor to take on a position as Medical Specialist. The department is part of Global Development and is responsible for the medical part of development of new drugs, devices and life cycle management of marketed drug and device products. The department consists of 11 Medical Specialists, 2 MDs in rotation program, 2 assistances and 1 PhD student.

The Job
The key responsibilities of the successful candidate will be to take the role as the medical expert within the assigned projects including medical review of key documents related to development and the design of the clinical development programme and/or devices in collaboration with marketing, regulatory affairs and other functions. You will be a driving factor in the cross-organisational implementation of clinical strategies, and have the medical responsibility during execution of trials. In addition, you will be responsible for providing high-quality input for new applications as well as feedback to questions posed by health authorities worldwide. Finally, you will maintain and chair a cross-functional scientific board of internal and, if required, external research colleagues involved in the different phases of the product development. The job is globally oriented and will require strong interaction with highly skilled colleagues and external stakeholders including treating physicians and therapeutic experts.

Qualifications
You have a medical degree and preferable knowledge within internal medicine including scientific training, e.g. a PhD degree. It will be regarded as an advantage, if you have documented expertise within drug and/or device development and experience in strategy planning from previous work in the pharmaceutical industry. You are a reliable, open-minded and dedicated team player, who thrives in a global environment of continuous development, and focuses on completion, quality and results. Interaction with internal and external experts require proficiency in English, high communication-, coordination-, and planning capacities, as well as flexibility and a keen sense of quality.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please call Per K Christensen on + 45 3079 1529.

Deadline
28 April 2014.

Denmark - Søborg Research & Development, Medical Doctor
21-Mar-2014 QA technician
Do you want to work with Quality Assurance and secure quality mind set in a complete supply chain. Do you like cooperate with our internal stakeholders all over the world and secure timely approval of materials...

QA technician

  • Quality
  • Denmark - Bagsværd

Do you want to work with Quality Assurance and secure quality mind set in a complete supply chain. Do you like cooperate with our internal stakeholders all over the world and secure timely approval of materials? Then we have the right job for you in Sourcing QA.

About the department
The open position as QA assistant is in the Primary Packaging Materials team that is responsible for quality and release of Primary Packaging Materials for all our production sites worldwide. The team also participants in development projects ensuring the availability of new high quality primary and secondary packaging materials for drugs and devices. The team consists of 9 QA professionals and 2 QA technicians.

The Job
You will work closely together with the 2 other QA technicians and be responsible for timely approval in novoLIMS, SAP/PRISM and support Novo Nordisk sites worldwide. Review of batch documentation and support the team in daily tasks such as data analysis, archiving and updating relevant GMP documentation.

We work in a dynamic and challenging environment with short deadlines you must be able to make prioritisations and take responsibility for customer requirements also when the solution is not obvious.

You must be capable of working independently and support the team – including optimising and standardising processes to ensure high level of quality and compliance in our team. We have a high focus on improvement of our processes both with regard to quality, costs and lead time.

Qualifications
You have a relevant technical or academic background e.g. laboratory technician, metrologist, bioanalyst or the like. You have a strong quality mind-set. Preferably you have worked in a GMP-compliant laboratory or with quality assurance in the pharmaceutical industry.

You like working with IT-systems, or even have experience with PRISM, SAP and novoLIMS or other relevant ERP-system.

You must be fluent in English, both written and spoken since we are cooperating broadly with many stakeholders.

As a person you are known for your positive mindset and you enjoy working in a dynamic environment with many simultaneous tasks and changing priorities.

We offer a very exciting job with excellent development opportunities among highly competent colleagues in a positive working environment.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development

Contact
For further information, please call Torben Herslund on + 45 3079 0956.

Deadline
4 May 2014.

Denmark - Bagsværd Quality
21-Mar-2014 Team Leader
Novo Nordisk is on a voyage towards the development and production of oral formulations of proteins. Our ambition is to develop break-through products based on orally available versions of insulin and GLP-1. Th...

Team Leader

  • Research & Development
  • Denmark - Måløv

Novo Nordisk is on a voyage towards the development and production of oral formulations of proteins. Our ambition is to develop break-through products based on orally available versions of insulin and GLP-1. That is why we are looking for a Team Leader who can take the lead for our team of skilled and dedicated employees. You will be involved in CMC activities for formulation/process development, pilot production, scaling up and analysis of solid protein dosage forms towards clinical trials.

About the department
We are 25 scientists and technicians in Oral Formulation & Process Development organised in two development teams. The department is responsible for the development of solid dosage form of insulin and GLP-1 analogues for oral delivery. The formulation development covers early phase development of oral protein formulations and processes in small scale to later stages of formulation development on a larger scale. We use rational design, statistical and QBD principles. You will report to the Director and will be member of the Management team in Oral Process and Formulation Development.

The job
You will manage a team of 10-15 highly skilled specialists, scientists and technicians, who develop, scale up and document oral protein formulations and processes for preclinical evaluation and clinical trials. The Process Development team’s main tasks are to set up and report on experimental designs in order to develop oral protein formulations and processes. Overall, you will play a key role in expanding our competency base within the solid dosage form process technology area.

Your key to success lies within your ability to perform as an inspiring, coaching and motivating manager and, at the same time, handle administrative tasks and contact to many stakeholders in a complex organisation. To obtain this, you lead and direct your employees on a daily basis and make sure that we have the right resources in the team. You will join a LEAN culture where continuous improvement is a natural part of our everyday work.

Qualifications
You have a Master’s degree in Engineering, Chemistry, Pharmacy or similar and solid experience from the pharmaceutical industry, ideally an international setting. Your experience as people manager has taught you how to pass your own passion on to your team in an involving and appreciative way. High-quality is a trademark for you, and you use LEAN as a naturally in your leadership. You have credibility, and you can make yourself understood and are able to realise your decisions. Finally, you must thrive in an environment where ongoing changes are a part of our business’ development.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please contact Lone Løgstrup Kimer at +45 3079 3569.

Deadline
22 April 2014.

Denmark - Måløv Research & Development
20-Mar-2014 Postdoctoral Researcher in Immunology
An international Postdoctoral position in the field of immunology of autoimmune diseases is available for a highly skilled and dedicated scientist, through collaboration between Novo Nordisk Research Center Sea...

Postdoctoral Researcher in Immunology

  • Research & Development
  • Denmark - Greater Copenhagen area

An international Postdoctoral position in the field of immunology of autoimmune diseases is available for a highly skilled and dedicated scientist, through collaboration between Novo Nordisk Research Center Seattle, USA and the Nuffield Department of Clinical Neurosciences, University of Oxford, UK.

About the department
The project will be mainly performed in the laboratory of Professor Lars Fugger, University of Oxford, where the Postdoctoral Researcher will join a team of scientists, clinicians and statisticians with a range of immunological expertise to work in an interdisciplinary research environment. The University of Oxford is a stimulating organization, which enjoys an international reputation as a world-class center of excellence in research and teaching.

The Novo Nordisk Research Center Seattle is home to the company’s Inflammation R&D Centre where researchers leverage Novo Nordisk’s strong knowledge within the field of proteins, in order to expand and enhance the company’s clinical pipeline of products for the treatment of chronic inflammatory diseases. Globally, about 6,000 Novo Nordisk employees are involved in research and development activities, with the main R&D facilities being located in the Copenhagen area (Denmark), Beijing and Seattle.

The Job
The project will focus on elucidating how immunological risk factors in autoimmune diseases, can be translated into gene function and how this can be utilised to improve the treatment of patients with autoimmune conditions. A combination of biochemical, molecular, cellular and immunological approaches will be used.

The successful candidate will be a Novo Nordisk employee. For the duration of the position the candidate will be primarily based in the laboratory of Professor Lars Fugger, University of Oxford, UK. In addition, there will be a unique opportunity to use state-of-the-art facilities in the Novo Nordisk Research Center Seattle, USA and to visit the Novo Nordisk research headquarters in Denmark. The position is for a fixed-term period of two years and is available as soon as possible. The recruitment process will be conducted cooperatively between Novo Nordisk and the University of Oxford. The position is offered as part of the Novo Nordisk R&D STAR programme (Science, Talent, Attraction and Recruitment). This programme supports the brightest graduate students in biotechnology, life, medical and engineering sciences, who want to pursue a career in pharmaceutical R&D.

Qualifications
A PhD in Immunology is essential, with up to 3 years postdoctoral research experience. Prior research experience investigating the immunological and/or genetic association of an autoimmune disease would be highly advantageous. The successful candidate must have excellent English language skills and be able to communicate results clearly as demonstrated by both oral presentation and a strong publication record. A capacity to show initiative in developing novel techniques and strategies to achieve research goals is also required.

At Novo Nordisk, we strive for excellence. Your curiosity, skills, dedication and ambition will help us change lives for the better. We offer you an opportunity to work in an extraordinary stimulating scientific environment.

Contact
For further information, please contact Jacques Peschon at JQPS@novonordisk.com or lars.fugger@imm.oxa.c.uk.

Deadline
16 April 2014

Denmark - Greater Copenhagen area Research & Development
20-Mar-2014 Process Engineer – SME Support
Device manufacturing & Sourcing (DMS) seeks an experienced engineer with experience within the field of validation and documentation of decoration and robots In this job, you will take up the position as Su...

Process Engineer – SME Support

  • Production
  • Denmark - Hillerød

Device manufacturing & Sourcing (DMS) seeks an experienced engineer with experience within the field of validation and documentation of decoration and robots

In this job, you will take up the position as Support Engineer for robot’s and decoration to our external component suppliers.

About the department
Process Support in Hilleroed is part of Device Manufacturing & Sourcing (DMS) and is responsible for the injection moulding and decoration of plastic components for devices such as Vagifem®, FlexPen® and the next generation of pre-filled devices. The department employs about 85 members of staff and faces a multitude of exciting challenges in the next few years with the launch of several new products.

The job
You will be measured against and take up the position as Support engineer for robots and decoration at one of our external suppliers. Your main tasks will be to ensure and maintain the communication flow, and support between the external supplier and our expert engineers in the team.

Besides that you will be expected to coordinate tasks and ensure timely planning and execution of activities at the supplier. Daily task will be: follow up on performance and structured problem solving, documentation, knowledge sharing, contact to supplier, and support the experts where needed.

Qualifications
You are an experienced engineer or similar within technical support. You have experience with similar challenges, have good fundamental technical skills and you are experienced in working with systematic problem solving.

You are outgoing, have strong communication skills and enjoy communicate with others.

As a person you can stay focused in a sometimes busy working day and you always approach tasks and colleagues with a positive attitude and energy.

You have a build-in quality mind-set – and have the ability to have an overall view of many tasks. Besides that you are able to do the above mentioned things with a smile and a positive approach.

The position is based at Moulding Equipment Support, a team of 20 engaged Engineers and Technicians, in the division of Device Manufacturing Sourcing, which employs approx. 400 people. DMS works within component manufacturing and pre-assembly of Novo Nordisk pre-filled insulin pens, and provides many exciting career development opportunities.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth. Your skills, dedication and ambition help us change lives for the better. In addition, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information please contact Jens Antonsen at +45 3079 2676.

Deadline
1 May 2014.

Denmark - Hillerød Production
11-Mar-2014 Senior QA Engineer
Are you ready to use your QA skills in Device Development projects in Novo Nordisk? As Senior Quality Engineer in Device Research & Development, DRD, you will use your knowledge and personality to make DRD ...

Senior QA Engineer

  • Quality, senior position
  • Denmark - Hillerød

Are you ready to use your QA skills in Device Development projects in Novo Nordisk?

As Senior Quality Engineer in Device Research & Development, DRD, you will use your knowledge and personality to make DRD develop superior products that help people every day all over the world.

About the department
DRD Quality is a six month old department and we are responsible for quality assurance of development activities from ideas until transfer to production. We are in close cooperation with project managers and Quality Assurance from other parts of Novo Nordisk and external partners. We also administrate the Quality Management System in DRD. You will join a group of nine skilled and engaged Quality Assurance engineers and specialists that work in the projects to secure compliance to procedures and regulations.

The Job
In DRD Quality we look for a skilled and motivated Senior QA Engineer that can support and influence project groups to help them meet the requirements from procedures and regulations. In the projects you will review and approve documentation on requirement engineering, safety risk management, design verification and design validation. You will also review and approve change requests and non-conformities. Device projects use a mix of technologies to make the best injections devices and you must be able to support device as well as primary packaging development activities.

Qualifications
You hold a relevant academic degree in engineering, pharmacy or equivalent and have relevant working experience ideally within combination products (drug/device). You have an up-to-date knowledge of relevant GMP requirements.

You are used to work in a team and are known to deliver according to targets. You make a difference, and by your dedicated and determined approach you complete your tasks in close cooperation with your colleagues. You work in a structured way and you get energized by learning new things. You are robust, can keep focus and you have the communication skills that are necessary to get alignment across multiple QA units. Quality is essential to you and incorporated in your daily work. On a personal level you are ambitious and have a great interest in developing yourself. You are fluent in both written and spoken English on a professional level.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please call Eva Petersson on +45 3075 9034.

Deadline
21 April 2014

Denmark - Hillerød Quality, senior position
04-Mar-2014 OHS Consultant – chemistry and biology
In this job, you will be part of a unit that supports a rapidly growing organisation globally to ensure that Novo Nordisk provides a healthy and safe working environment for all. If you find challenges like thi...

OHS Consultant – chemistry and biology

  • Human Resources
  • Denmark - Bagsværd

In this job, you will be part of a unit that supports a rapidly growing organisation globally to ensure that Novo Nordisk provides a healthy and safe working environment for all. If you find challenges like this exciting and inspiring, you may be our new Occupational Health and Safety Consultant.

About the department
The job is located in Corporate Occupational Health and Safety (COHS) which is a corporate staff function and a part of Corporate People & Organisation situated in Bagsværd. COHS is Novo Nordisk's Centre of Excellence in the field of global occupational health and safety with 28 dedicated colleagues within ergonomics, psycho-social and technical working environment. COHS’s role is to inspire and support the OHS work throughout the global organisation, and thereby enabling line of business to realise Novo Nordisk’s OHS ambitions by providing easy-to-use guidance, tools and data.

The job
Your main responsibility will be general OHS counseling and counseling in the field of chemistry, toxicology and biology. This will be done by developing and providing the organisation with methods, guidelines, standards and tools on chemical, toxicological and biological issues as well as sharing better practice across the organisation globally. You will play a key role in ensuring compliance in regard to chemicals and biological materials including genetically modified organisms (GMO) and approvals hereof from authorities in Denmark. Your counseling will be based on your field of expertise knowledge, regulatory requirements, good practice and Novo Nordisk’ values.

To make sure that the organisation is heading in the right direction and to meet the ambitious targets, general OHS consultancy is also part of the job. Furthermore you will participate in and drive minor OHS projects and in planning and performing the training of the OHS organisation.

Qualifications
You hold a B.Sc. or a M.Sc. in chemistry, engineering or equivalent with strong focus on occupational health and safety. You have at least three years of experience within health and safety with focus on chemistry and biology preferably from an international company with production facilities.

You have a high level of drive and work well in a dynamic environment. You adapt easily to changes and shifting demands and are eager to contribute to the continuous development of the area.

You are result-oriented, like to be challenged and are able to conceptualize ideas into simple and standardised tangible business concepts. You have a well-structured approach to your tasks and are capable of maintaining an overview also under time pressure. Furthermore, you have excellent communication and stakeholder management skills.

English is our corporate language, and hence it is a prerequisite that you speak and write English fluently. You work comfortably in MS Office. It is also important that you are able to stay focused in a sometimes busy working day and that you approach tasks and colleagues with a positive attitude, energy and good humour.

At Novo Nordisk, decisions and actions are based on their impact on society, the environment and on their potential to generate a profit. That makes for a responsible culture with a healthy and engaging working environment.

Contact
For further information, please contact Director Nina Gylche Møller at +45 3079 4756.

Deadline
30 April 2014.

Denmark - Bagsværd Human Resources

Vacant positions posted in Danish/Ledige stillinger på dansk

Opslået Jobtitel Sted Kategori
16-Apr-2014 Lab. tech for analysis support
Kopier stillingsopslaget ind i dette felt, når stillingen er klar til annoncering...

Lab. tech for analysis support

  • Forskning og Udvikling
  • Danmark - Måløv

Kopier stillingsopslaget ind i dette felt, når stillingen er klar til annoncering

Danmark - Måløv Forskning og Udvikling
16-Apr-2014 Laborant til laboratorieforsøg/produktion af HPLC-kolonner
Vil du samarbejde omkring stabile produktionsprocesser og levering af HPLC-kolonner og være en del af et team i udvikling med fokus på faglighed, engagement og quality mindset ? Du er positiv, engageret og flek...

Laborant til laboratorieforsøg/produktion af HPLC-kolonner

  • Forskning og Udvikling
  • Danmark - Køge

Vil du samarbejde omkring stabile produktionsprocesser og levering af HPLC-kolonner og være en del af et team i udvikling med fokus på faglighed, engagement og quality mindset ? Du er positiv, engageret og fleksibel, og du trives med en omskiftelig hverdag, hvor fokus sættes ud fra kundernes behov. Vi har brug for din hjælp i en 6-7 måneders periode. Vi tilbyder en spændende arbejdsplads med skiftende udfordringer, hvor du kan opnå god erfaring med kolonneproduktion/stabilisering af produktionsprocesser. Arbejdet foregår i en uformel atmosfære, hvor vi har fokus på som team at levere i rette kvalitet til vores kunder.

Om afdelingen
FeF Chemicals A/S er et 100% ejet datterselskab af Novo Nordisk A/S og ligger i Køge. I dag er vores største produktgruppe substitueret kiselgel, der bruges til kromatografisk oprensning af Novo Nordisks lægemidler. Desuden producerer vi kvaternære ammoniumforbindelser, som vi markedsfører over hele verden. Vi er i dag ca. 140 ansatte i firmaet. Udviklingsafdelingen består af 7 kemikere og 15 laboranter fordelt på 3 teams. Vi er kompetencecenter for gelteknologi i Novo Nordisk, hvilket indebærer en tæt kontakt til forsknings-, udviklings- og produktionsafdelinger i koncernen.

Du bliver en del af Kolonnepak-teamet, som består af 5 laboranter, 4 kemikere og en teamleder.

Teamet producerer analytiske HPLC-kolonner til analyse af lægemidler og brug i udviklings-, produktionsudvikling- og analyseafdelinger i Novo Nordisk og FeF. For at stabilisere kolonneproduktionen gennemfører vi udviklingsprojekter, baseret på laboratorieforsøg. Vi fremstiller kromatografiske faser ved organisk syntese med kiselgel og producerer kolonner under ISO9001. Tungt fysisk arbejde kan forekomme. Såvel udvikling som produktion dokumenteres.

Jobbet
Arbejdet vil hovedsagelig bestå i at udføre og dokumentere laboratoriearbejde omkring levering af HPLC-kolonner og stabilisering af produktionsprocesser for kromatografiske geler og kolonnepakning.

Vi producerer, pakker og kvalitetskontrollerer kolonner. Du vil afhængig af erfaring komme til at udføre kemiske udviklingsforsøg med geler og kolonner/arbejde med forskellige produktionsprocesser og i mindre omfang kvalitetskontrol samt indgå i vedligehold og rengøring af udstyr. Du vil have kundekontakt, deltage i planlægning, dokumentere og håndtere ordrer, herunder udføre PC-arbejde. Du vil opleve, at vi fokuserer på LEAN principper, og du vil kunne bidrage til at optimere vores arbejdsgange omkring kolonner.

Kvalifikationer
Du er uddannet (industri) laborant med erfaring indenfor HPLC-analyse og dokumentation (ISO/GMP). Det er en fordel, hvis du har kendskab til organisk syntese.

Du er god til at planlægge og organisere din arbejdsdag. Som person er du omhyggelig og samvittighedsfuld omkring udførelsen af dine arbejdsopgaver. Det er vigtigt, at du har en god ordenssans. Du skal være indstillet på at lære nye måder at gøre tingene på og være en engageret teamspiller, der gerne viser vejen i samarbejde med kollegerne.

Som person har du let ved at omgås kolleger på alle niveauer i organisationen, og du gør dit for at bidrage til den positive stemning i teamet. Du er selvstændig og tager styring over egne opgaver, og du trives med at løse opgaverne i tæt samarbejde med dine kolleger. Du tager ansvar for, at vi både som team og individer, når de mål forretningen har brug for. Du kan lide at optimere arbejdsgange og er god til at afslutte opgaver.

Hvis du er indstillet på at dokumentere levering af HPLC-kolonner og stabile produktionsprocesser, kan vi tilbyde dig samarbejde med kompetente og engagerede kolleger og mulighed for professionel og personlig udvikling.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, er du meget velkommen til at kontakte Kirsten Modvig på +45 2429 4119

Ansøgningsfrist
21. april 2014

Danmark - Køge Forskning og Udvikling
16-Apr-2014 QC Supporter
Har du erfaring med GMP og kan du håndtere så forskelligartede opgaver som projektledelse, afvigelseshåndtering, problemløsning og dokumentskrivning? Trives du desuden med at arbejde med kvalitetskontrol? Hvis ...

QC Supporter

  • Produktion
  • Danmark - Bagsværd

Har du erfaring med GMP og kan du håndtere så forskelligartede opgaver som projektledelse, afvigelseshåndtering, problemløsning og dokumentskrivning? Trives du desuden med at arbejde med kvalitetskontrol? Hvis svaret er ja, kan du måske være vores nye QC Supporter.

Om afdelingen
Du vil blive en del af QC Packaging Materials i Bagsværd. Vi er ansvarlige for kvalitetskontrol af trykte- og primære pakkematerialer til produktionsafdelinger i Danmark og resten af verden. Vores fokus er at levere høj kvalitet til de aftalte deadlines – hver gang. I dag er vi 41 dedikerede medarbejdere i to teams, og den aktuelle stilling ligger i QC Printed Pack teamet.

Jobbet
Dine overordnede mål i jobbet er at sikre compliance og nå deadlines for afdelingens opgaver indenfor både kvalitet og levering af trykte pakkematerialer. Du koordinerer og er operationelt ansvarlig for projekter, hvor du definerer milestones og sikrer at vi når de aftalte deadlines. Du er ansvarlig for forbedringsprojekter i afdelingen og deltager i tværorganisatoriske grupper. Du får en vigtig rolle i at supportere QC-assistenterne i deres daglige arbejde og i at sikre at vores måleudstyr lever op til gældende krav for området. Derudover er håndtering af afvigelser og dokumentskrivning andre vigtige opgaver. Generelt kan du se frem til et spændende, alsidigt og udfordrende job.

Kvalifikationer
Du har en akademisk uddannelse sandsynligvis indenfor naturvidenskab. Du har erfaring fra GMP, og måske tilmed praktisk erfaring med kvalitetskontrol. Derudover er du interesseret i kalibrering og validering af IT-baserede kvalitetskontrolsystemer. Hvis du ikke allerede har praktisk erfaring med LEAN er du motiveret for at lære det. Du er struktureret og analytisk, kan identificere årsager og efterfølgende tilpasse metoder/procedurer/processer for at forebygge at problemet vender tilbage. Du trives med at have kontakt til mange mennesker, og du bruger dine gode kommunikationsevner til at skabe gode relationer til interessenter. For at lykkes i jobbet er det vigtigt, at du kan arbejde selvstændigt og planlægge dine egne opgaver. Du taler og skriver flydende dansk og du mestrer engelsk på professionelt niveau.

Hos Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Michael Lange +45 3079 1995.

Ansøgningsfrist
4. maj 2014

Danmark - Bagsværd Produktion
15-Apr-2014 Operatør til Basisvareproduktion
Tør du prøve kræfter med vores avancerede procesanlæg, som kræver, at du kan overskue stor kompleksitet? Vil du være med til at sikre, at vores produkter kommer godt fra start i en højkvalitet API produktion? K...

Operatør til Basisvareproduktion

  • Produktion
  • Danmark - Kalundborg

Tør du prøve kræfter med vores avancerede procesanlæg, som kræver, at du kan overskue stor kompleksitet? Vil du være med til at sikre, at vores produkter kommer godt fra start i en højkvalitet API produktion? Kan du holde overblikket og bevare roen i en hverdag, som er omskiftelig og foregår i et højt tempo?

Så er du måske den nye engagerede kollega, vi søger i Diabetes API, Insulin Manufacturing 1, Kalundborg. Vi er et team med 40 operatører, som varetager produktion af Insulin Aspart og kampagneproduktioner for CMC.

Stillingen er en fast stilling.

Vi har styr på proces og udstyr
Du kan se frem til en hverdag med mange og varierede arbejdsopgaver, men hovedvægten i jobbet ligger på udførelse af processtyring herunder fejlsøgning, rengøring af procesudstyr samt forskellige ad hoc opgaver.

I afdelingen har vi meget fokus på kvalitet. Derfor arbejder vi hele tiden med at sikre et højt kvalitetsniveau og udfører således løbende dokumentation af vores arbejde. Det bliver også din opgave at sørge for, at produkterne lever op til kvalitets- og myndighedskrav herunder GMP, som er en forudsætning for vores produktion. Vi arbejder med daglig målstyring, og cLEAN® er en vigtig del af vores hverdag.

Du vil i det daglige arbejde få en bred kontaktflade med kolleger fra andre teams i afdelingen som f.eks. teknikere og kemikere.

Vi arbejder i tre-holdskift, 7 dage om ugen, og der er gennemsnitligt weekendvagt hver 2. uge.

Initiativ og kvalitetssans
Du har gerne erfaring med at arbejde i en produktion og kender måske til GMP, men din faglige baggrund er ikke så væsentlig. Det vigtigste er, at du tager ansvar og er meget bevidst om kvaliteten i alt dit arbejde. Du er handlingsorienteret og viser initiativ ved selv at byde ind og drive opgaver. Samtidig har du lyst til at arbejde i et miljø, hvor der kræves en stor del dokumentation.

Du skal også være klar til løbende at tilegne dig nye færdigheder og håndtere de udfordringer og forandringer, som ligger foran dig. I vores team er samarbejde vigtigt, så du skal have en positiv indstilling og lysten til at løse opgaver i fællesskab med kolleger.

For at kunne begå dig i vores produktion skal du have lyst og evne til at arbejde med mange forskellige typer procesudstyr, have teknisk flair og være fortrolig med brug af IT.

Kontakt
Vil du vide mere om stillingen, så kontakt Claes Tinglev Åside på + 45 3075 0416.

Ansøgningsfrist
22. april 2014

Danmark - Kalundborg Produktion
15-Apr-2014 Akademiker til IM2 Fermentation Support, Kalundborg
Brænder du for et job i et travlt produktionsmiljø? Kan du lide at lave grundig og systematisk problemløsning på baggrund af data, ved brug af LEAN-værktøjer, og trives du med at arbejde på tværs af faggrænser?...

Akademiker til IM2 Fermentation Support, Kalundborg

  • Produktion
  • Danmark - Kalundborg

Brænder du for et job i et travlt produktionsmiljø? Kan du lide at lave grundig og systematisk problemløsning på baggrund af data, ved brug af LEAN-værktøjer, og trives du med at arbejde på tværs af faggrænser? Så er du måske den akademiker vi søger til vores gæringssupport team.

Om afdelingen
Vil du være med til at sikre kvaliteten af insulinprodukter på de allerførste trin i produktionsprocessen? Så er du måske vores nye kollega i afdelingen Fermentation, hvor vi har ansvaret for både gæringsproces, utilitysystemer og produktionsudstyr. Dit team består af supportere med både tekniks og akademisk baggrund, som konstant overvåger procesafvikling, gæringstanke og de fysiske anlæg i fabrikken – Insulin Manufacturing II (IM2) i Kalundborg. Glæd dig til et job, hvor du er med til at gøre en forskel for produktionen af bl.a. human insulin og moderne insuliner.

Jobbet
Sammen med teamet får du ansvaret for at sikre, at produktkvaliteten er i orden i henhold til gældende myndighedskrav. Dine primære opgaver bliver bl.a. at overvåge og søge fejlårsager og trends i processen via vores it-systemer, ligesom du udarbejder SOPs, e-logs, reviews og afvigelsesrapporter. Du opretter ændringssager og sparrer med dine kolleger i vedligeholdsafdelingen. Desuden kommer du til at deltage i og drive mindre og større projekter med henblik på at optimere vores udstyr og processer. Vi arbejder indgående med Lean, og på vores daglige tavlemøder bidrager du med ideer til at sætte struktur på vores problemløsning og igangsætte f.eks. workshops. Du kan se frem til en stilling, hvor du får rig mulighed for at udvikle dine personlige og faglige kompetencer og sætte dit præg på samarbejdet i afdelingen. Jobbet indebærer specifikt ansvaret for vores vand- og dampanlæg. Det er således dit ansvar at følge op på kvaliteten af vand og damp, som har stor fokus i afdelingen, og foretage årlige afrapporteringer af dette. Som ansvarlig for vand/damp vil du endvidere blive en del af procesgruppe på tværs af Diabetes API, hvor du vidensdeler og harmoniserer med øvrige fabrikker i DAPI.

Kvalifikationer
Din baggrund er en relevant akademisk uddannelse og gerne erfaring fra kemisk, farmaceutisk eller fødevareproduktion. Du har god forståelse for samspillet mellem proces og udstyr og kendskab til GMP eller et lignende kvalitetssystem. Med andre ord er du yderst kvalitetsbevidst, og har du erfaring med optimering af såvel produktion som administrative processer, er det en fordel. Dine kolleger eller studiekammerater kender dig som en engageret og positiv person, der er meget bevidst om sit ansvar. Du kan både arbejde selvstændigt og indgå i tæt samarbejde – også selvom det er på tværs af team og faggrænser. Endelig interesserer du dig for Lean, og du er positivt indstillet over for forandringer, da du er god til at se muligheder frem for begrænsninger.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Thomas Neergaard på + 45 3075 3994

Ansøgningsfrist
4. maj 2014

Danmark - Kalundborg Produktion
15-Apr-2014 Studentermedhjælper
Studentermedhjælper til Steno Center for Sundhedsfremme Vil du være med til at udvikle nye tilgange til at forebygge diabetes? - og har du lyst til at være en del af et konkret forsknings- og udviklingsprojekt...

Studentermedhjælper

  • Studerende
  • Danmark - Gentofte

Studentermedhjælper til Steno Center for Sundhedsfremme

Vil du være med til at udvikle nye tilgange til at forebygge diabetes? - og har du lyst til at være en del af et konkret forsknings- og udviklingsprojekt om sundhedsfremme? Så skal du måske være vores studentermedhjælper?

Steno Center for Sundhedsfremme er et forskningscenter, som udvikler ny viden, metoder og tilgange til sundhedsprofessionelle og andre aktører, som kan skabe bæredygtig social forandring til fremme af folkesundheden i relation til diabetes. Centeret integrerer social- og humanvidenskabelig forskning for at skabe nye tilgange på et område, som trænger til at blive videnskabeligt fornyet. Centerets ambition er at udvikle et nationalt og internation¬alt kraftcenter med fokus på social forandring.

SoL Odsherred – Sundhed og Lokalsamfund

Steno Center for Sundhedsfremme fokuserer på forebyggelse af type 2 diabetes med udgangspunkt i børnefamilier og lokalsamfund. Inspireret af supersetting konceptet, som arbejder med sundhedsfremme baseret på synergier mellem forskellige arenaer (settings), søger SoL at fremme sundhed og trivsel blandt familier med små børn i tre lokalsamfund i Odsherred Kommune. Projektet implementeres i samarbejde med Aalborg Universitet og Forskningscenter for Forebyggelse og Sundhed i Glostrup.

Stillingen

På Steno Center for Sundhedsfremme, Steno Diabetes Center, søger vi en studentermedhjælper til SoL Odsherred projektet. Arbejdet vil omfatte forskellige opgaver, som litteratursøgning, transskription, mødeforberedelse og arbejde med videnskabelige manuskripter. Der vil dog i den første tid være hovedvægt på gennemførelsen af semi-strukturerde interviews i forbindelse med en interessent-analyse i Odsherred Kommune. Ansættelsen er i gennemsnit tre dage om ugen i Forebyggelsesgruppen ved Steno Center for Sundhedsfremme og vil vare til udgangen af 2014. Der må påregnes en øget arbejdsindsats i de første måneder. Dele af arbejdet vil foregå i Odsherred Kommune.

Din profil

• Du har en bachelor i et relevant fag, fx folkesundhedsvidenskab, sundhedsfremme, pædagogik, sociologi, antropologi, idræt eller psykologi.

• Du har solid erfaring med brug af kvalitative metoder herunder interviews.

• Du er dygtig, ambitiøs, motiveret, selvstændig, kreativ, engageret, resultatorienteret og en god kollega.

• Du har faglig og menneskelig modenhed og kan både arbejde selvstændigt og i et tæt samarbejde i en tværfaglig gruppe, hvor en positiv indstilling og humoristisk sans er afgørende.

• Du er tolerant og kan kommunikere med folk med forskellig baggrund.

• Du mestrer til fulde dansk og engelsk i skrift og tale.

Det er fordel, hvis du har erfaring med at:

• arbejde på forskningsprojekter.

• arbejde med feltarbejde i institutioner.

• arbejde i tværfaglige miljøer.

• arbejde med børn, familier og sundhedsfremme.

Ansøgning

Din ansøgning, på dansk eller engelsk, skal indeholde:

• Din motivation og baggrund for at søge stillingen (max 1 side)

• CV (max 2 sider)

Ansøgningen sendes elektronisk senest torsdag 1. maj 2014, kl. 12.00. Stillingen ønskes besat snarest muligt.

Kontakt

Yderligere information fås fra Paul Bloch (50926617).

Om Steno

Steno Diabetes Center er en af verdens førende institutioner inden for diabetesbehandling og forebyggelse. Steno ejes af Novo Nordisk A/S og er en 'not for profit' virksomhed, der arbejder i partnerskab med det danske sundhedssystem. Steno står for behandlingen af ca. 5.600 mennesker med diabetes. For yderligere oplysninger, se www.steno.dk.

Danmark - Gentofte Studerende
15-Apr-2014 Kvalificerings og- valideringsekspert til strategisk vigtig satsning
Vil du være en del af et innovativt produktionsmiljø, hvor vi pakker Novo Nordisks hæmofili-produkter og aldrig går på kompromis med kvalitet? Har du solid erfaring med kvalificering af udstyr og /eller valider...

Kvalificerings og- valideringsekspert til strategisk vigtig satsning

  • Produktion
  • Danmark - Kalundborg

Vil du være en del af et innovativt produktionsmiljø, hvor vi pakker Novo Nordisks hæmofili-produkter og aldrig går på kompromis med kvalitet? Har du solid erfaring med kvalificering af udstyr og /eller validering af processer på brugersiden fra medicinalbranchen? Og er du klar til en ekspertrolle, hvor du sætter din GMP viden helt i front til gavn for kolleger og patienter over hele verden? Så kan du meget vel være vores nye Kvalificerings- og proces supporter.

Biopharms nye pakkeri er en strategisk vigtig satsning, der skal sikre den fremtidige kapacitet til at pakke Novo Nordisks hæmofili-produkter samt GlucaGen® Hypokit. Det giver et dynamisk arbejdsmiljø, hvor vi på samme tid skal sikre stabile leverancer af livsvigtig medicin til vores kunder, håndtere forberedelsen af en ny pakkelinie samt støtte og udføre flere projekter i afdelingen.

Om afdelingen
Afdelingen i Biopharm, Finished Products består pt. af ca. 60 dygtige medarbejdere, der alle beskæftiger sig med pakning af NovoSeven® og NovoEight® og på sigt flere hæmofiliprodukter og GlucaGen® Hypokit. Afdelingen er relativ ny og forventes ligeledes at vokse betragteligt over de kommende år. Afdelingen er opdelt i tre teams; et produktions team, et proces support team og et teknisk support team. Du vil indgå i proces support teamet, hvor dine kommende kolleger består af akademikere og laboranter.

Jobbet
I Biopharm lægger vi vægt på, at alle tager et personligt ansvar for kvalitet, opgaver og hinanden. Vi sætter ambitiøse mål, samtidig med at vi fokuserer på stabil leverance til vores kunder. Din primære opgave er at være overordnet ansvarlig på bruger siden, når processerne skal valideres samt sikre kvalificering af vores udstyr. Både ved revalideringer og efterhånden som vi bygger vores produktion op.

Du vil fungere som afdelingens valideringsekspert ved inspektioner og audits. En del af dit arbejde vil også bestå i support til produktionen, udarbejdelse af afvigelser og frigivelse af vores produkter. Din arbejdsdag vil således blive afvekslende og til tider hektisk, da driften af vores fuldautomatiserede pakkelinje er essentiel for gennemførelse af produktionen. Arbejdet vil foregå i tæt dialog med mange medarbejdergrupper både i og udenfor afdelingen. Det betyder, at vi stiller lige store krav til selvstændighed og det at være en god teamplayer.

Kvalifikationer
Til tiltrædelse snarest søger vi en kollega, der har en solid baggrund indenfor kvalificering og/eller validering. Den ideelle kandidat har minimum 5 års erfaring indenfor færdigvareproduktion af medico- eller medicinalprodukter og en stor og dokumenteret forståelse for GMP. Du har en relevant uddannelsesmæssig baggrund som farmaceut, produktions-, kemi- eller maskiningeniør.

Du er en stærk kommunikator, der bliver lyttet til, når vi taler kvalificering, og er rigtig god til at formidle denne viden til andre. Du er vant til at arbejde selvstændigt, tage ansvar og finde løsninger i selv pressede situationer. Samtidig sikrer du involvering og ejerskab blandt dine kolleger, og er god til at etablere samarbejde på tværs af faggrænser. Du er åben og ærlig, og i stand til at give og modtage konstruktiv feedback. Vi arbejder i en GMP reguleret virksomhed, hvorfor du lægger vægt på detalje, struktur og kvalitet i dit arbejde.

Da Novo Nordisk A/S er en international virksomhed, er det et krav, at du behersker engelsk og dansk, såvel mundtligt som skriftligt.

I Novo Nordisk stræber vi efter at være de bedste. Vi er førende i verden indenfor diabetesbehandling og en større spiller indenfor behandling af blødninger, behandling med væksthormon og behandling med hormonterapi. Vi giver vores medarbejdere mulighed for en stærk professionel udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Nanna-Freja Riis Larsen på + 45 3079 1736.

Ansøgningsfrist
28. april 2014

Danmark - Kalundborg Produktion
15-Apr-2014 Kvalitetsassistent til Pilot Plant
Her er muligheden for at bruge din viden inden for GMP og kvalitetssystemer til at hjælpe Chemical Supply Pilot udvikle og fremstille næste generations lægemidler. Om afdelingen...

Kvalitetsassistent til Pilot Plant

  • Kvalitetssikring
  • Danmark - Bagsværd

Her er muligheden for at bruge din viden inden for GMP og kvalitetssystemer til at hjælpe Chemical Supply Pilot udvikle og fremstille næste generations lægemidler.

Om afdelingen
Chemical Development er vi 40 medarbejdere, som er organiseret i 3 teams og geografisk placeret i både Måløv og Bagsværd. Vi er ansvarlige for udvikling og opskalering af kemiske processer til support af til prækliniske og kliniske studier. Afdelingen dækker over en bred vifte af procesteknologier fra klassisk organisk syntese over fastfase syntese til kromatografisk oprensning. I teamet Chemical Supply Pilot er vi 17 kollegaer der sammen er ansvarlige for afvikling af pilotproduktioner, indsamling af procesdata samt optimering af fremstillingsprocesserne.

Jobbet
Som QMS assistent i afdelings pilot team, Chemical Supply Pilot, bliver du involveret i den daglige support til GMP produktion af API og mellemprodukter. Du vil få en bred vifte af ansvarsområder og opgaver i forbindelse med den daglige support.

Dit primære ansvarsområde som QMS assistent vil være det daglige ansvar for kvalitets-sikringsarbejdet, dvs. ansvarlig for at planlægge, opbygge og monitorere kvalitetssystemet i afdelingen. Endvidere har QMS assistenten ansvaret for at vedligeholde og effektivisere afdelingens kvalitetssystem og sammen med andre QMS repræsentanter være med til at vedligeholde og effektivisere områdets kvalitetssikringssystem.

I det daglige samarbejder du med en lang række af vores kollegaer, for at sikre compliance af processer og udstyr. Du er erfaren i brugen af IT systemer der understøtter den daglige GMP drift ift. den supporterende del, som dokumentation og kvalitet. Du er kvalitetsbevidst og en person der trives med opgaver som er en blanding af foranderlig og rutinemæssig karakter.

Kvalifikationer
Du har flere års erfaring med kvalitets arbejde inden for den farmaceutiske industri og har en teknisk baggrund (procesteknolog, farmakonom, laborant eller tilsvarende). Du er velorganiseret og trives med at der er orden og struktur i dokumentation og systemer.

Du har med fordel kendskab til de IT systemer der benyttes til kvalitetssikring inden for NovoNordisk (IsoTrain/QBIQ, LIMS, Omnirim mm) samt gerne kendskab til miljømonitorering af klassificerede områder.

På det personlige plan trives du med en høj grad af fleksibilitet – og med din evne til at omstille dig, befinder du dig rigtig godt i en stilling, hvor dagene ikke ligner hinanden. Du er struktureret, en god planlægger og har stort fokus på kvalitet i dit arbejde. Samtidig sætter du pris på en uformel tone og tæt samarbejde i teamet. Du er engageret, tager initiativ og søger selv udfordringer, du har et ”can do mind-set”.

I Novo Nordisk baseres beslutninger og handlinger på deres indflydelse på samfundet, miljøet og muligheden for at skabe økonomisk overskud. Det skaber tilsammen en ansvarlig kultur med et sundt og engageret arbejdsmiljø.

Kontakt
Vil du vide mere om stillingen, så kontakt Henrik Svane på + 45 3075 5695 eller Thomas Pittelkow på + 45 3079 3936

Ansøgningsfrist
9. maj 2014

Danmark - Bagsværd Kvalitetssikring
15-Apr-2014 Teamleder
Er du klar til at lede og motivere et team af højt kvalificerede kollegaer i et team, der arbejder med support til Biopharm AP produktioner i Gentofte og Kalundborg og sikre konsistens imellem både nye og marke...

Teamleder

  • Produktion
  • Danmark - Gentofte

Er du klar til at lede og motivere et team af højt kvalificerede kollegaer i et team, der arbejder med support til Biopharm AP produktioner i Gentofte og Kalundborg og sikre konsistens imellem både nye og markedsførte produkter? Kan du sætte en klar retning for dit team og fungere som en inspirerende sparringspartner for dine medarbejdere? Kan du bevare roen og prioritere opgaver i et dynamisk og hektisk miljø? Så har vi en stor mulighed for dig i Biopharm AP support.

Om afdelingen
I Biopharm AP Support er vi mere end 50 kompetente kolleger, der yder support til de forskellige AP produktionsprocesser inden for Biopharms portefølje bestående af hæmofiliprodukter, Norditropin ® og GlucaGen ®. Afdelingen fungerer som et bindeled mellem udvikling og produktion, så vi har fingeren på pulsen i alle de spændende nye og markedsførte produkter i Biopharms pipeline. Afdelingen er i dag opdelt i to teams, men da afdelingen fortsat vokser, etablerer vi nu et tredje team med ansvar for en kombination af nye og markedsførte produkter. Dit job bliver at lede dette nye team og være en del af den daglige ledelse i afdelingen. Afdelingen er placeret i Gentofte.

Jobbet
Som teamleder i det nye team, kommer du til at lede et team på ca. 13-15 fagligt dygtige og kompetente medarbejdere. De vigtigste opgaver bliver at sikre koordinering og prioritering af support til AP produktionerne, håndtering og koordinering af produkt-og procesorienterede opgaver samt sikre svar på spørgsmål fra myndighederne.

Nøglen til succes ligger i din evne til at en være en inspirerende, coachende og motiverende leder, der på samme tid, kan håndtere administrative opgaver og kontakt til mange interessenter i en kompleks organisation. For at opnå dette, skal du lede dine medarbejdere på daglig basis, og sørge for, at vi har de rigtige ressourcer i teamet.

Du spiller også en væsentlig rolle i løbende at skabe forbedringer gennem brugen af LEAN, så vi hele tiden optimerer vores arbejdsprocesser. Det gør du bl.a. gennem målstyring, systematisk problemløsning og opfølgning på efterlevelse af standarder. Du kan se frem til et miljø, hvor der hele tiden sker noget, og hvor du hver dag skal træffe vigtige beslutninger i forhold til levering, prioritering og skarpe deadlines.

Kvalifikationer
Du har en baggrund, som farmaceut, ingeniør eller tilsvarende, suppleret med solid erfaring i farmaceutisk produktion, der arbejder i overensstemmelse med GMP/ISO. Du har en naturlig interesse i personaleledelse og dit CV afspejler minimum 5 år ledelsesmæssig erfaring.

Du har en god sans for planlægning, arbejder systematisk og struktureret og er i stand til at opretholde det generelle overblik. Det er vigtigt, at du kender værdien af at skabe tillid og respekt fra kolleger og medarbejdere og ved, hvordan man kan motiverer sine medarbejdere i en travl og skiftende hverdag. Du har gode kommunikationsevner på dansk og engelsk. Du er i stand til at dele viden på ethvert organisatorisk niveau, og med din udadvendte og proaktive indstilling kan du nemt oprette et netværk på tværs af organisationen. Endelig har du et vågent øje for kvalitet og formår at prioritere dit arbejde til at opfylde enhver deadline.

Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

I Novo Nordisk, Biopharmaceuticals, bruger vi vores kompetencer, engagement og ambition om at hjælpe mennesker med hæmofili og væksthormonmangel og ændre deres liv. Ved at arbejde sammen med os, vil du have mulighed for at gøre det samme i et globalt erhvervsmiljø.

Kontakt
Vil du vide mere om stillingen, så kontakt Martin Arendt Petersen på + 45 3079 8228

Ansøgningsfrist
30. april 2014

Danmark - Gentofte Produktion
15-Apr-2014 Processupporter
Brænder du for aseptisk produktion og vil du arbejde hos verdens førende insulinproducent? Vi mangler en dygtig kollega til at supportere vores aseptiske fyldeproduktion. Grib muligheden for et job med masser a...

Processupporter

  • Produktion
  • Danmark - Bagsværd

Brænder du for aseptisk produktion og vil du arbejde hos verdens førende insulinproducent? Vi mangler en dygtig kollega til at supportere vores aseptiske fyldeproduktion. Grib muligheden for et job med masser af udvikling, en afvekslende hverdag med stor indflydelse og ansvar i en international virksomhed.

Om afdelingen
I afdelingen er vi ca. 70 medarbejdere, hvoraf vi er 10 processupportere, som dagligt yder support til en af vores fyldelinjer. Afdelingen består af operatører, teknikkere, ingeniører, farmaceuter og kemikere som alle arbejder tæt sammen og på tværs af flere afdelinger.

Vores fornemmeste opgave er at sikre vores produktion køre 24/7 og altid levere insulin til vores kunder i rette kvalitet og til rette tid.

Jobbet
Din vigtigste opgave bliver at yde en god og effektiv support så vi sikre en stabil drift af vores aseptiske fyldeproces. Undervejs vil du skulle bidrage til at løse en bred vifte af opgaver lige fra procesforbedringer, valideringer, systematisk problemløsning og afvigelsessager.

Når der opstår udfordringer i vores produktion, er det dig, der sikrer overblikket, så problemerne kan løses effektivt og korrekt. Du spiller således en nøglerolle i arbejdet med at sikre driften og samtidig være garant for frigivelse af vores produkter.

En stor del af dit arbejde vil foregå i samarbejde med andre hvor sparring og udveksling af ideer og viden vil være essentiel for opgaveløsningen. Du vil også skulle byde ind med viden og evner når det kommer til compliance og kvalitet så vi altid lever op til gældende myndighedskrav.

Som Aseptisk Processupporter kan vi tilbyde dig et udfordrende og innovativt miljø med gode muligheder for både personlig og faglig kompetence udvikling. Du vil opleve et godt sammenhold og et fælles ønske om at sørger for vores patienter for deres medicin.

Kvalifikationer
Du har en relevant naturvidenskabelig uddannelse som produktions-, miljøkemi- eller kemiingeniør, cand. scient el. lign. Du har et stort indblik i proteinkemi og aseptisk produktion. Desuden har du et godt kendskab til GMP/ISO reglerne og erfaring med audits.

Du besidder flere års erfaring fra lignende stilling, og det falder dig naturligt at tage ansvar, sætte retning og træffe beslutninger for dig selv og dine kollegaer i det daglige arbejde.

Du har evt. før været projektleder, haft ansvar for dele af produktionsprocesser eller andre tværgående processer, som gør, at du har et naturligt overblik og drive. Derudover har du solidt kendskab til LEAN, og det er en selvfølge for dig at bruge problemløsningsværktøjer i dit daglige arbejde. Samtidig skal du have lyst til at facilitere, udfordre og hjælpe dine kollegaer med brugen af disse værktøjer i hverdagen, så vi fortsat løfter vores høje niveau.

Du kommunikerer klart og tydeligt på både dansk og engelsk. Du er mål- og ansvarsbevidst og har viljen til at gå forrest både fagligt og i samarbejdet med alle faggrupper. Du er nysgerrig og udfordrende, og du tør tage styringen og danne dig et overblik ved f.eks. tværgående projekter og systematisk problemløsning. Ligeledes skal du kunne lære fra dig og være indstillet på indimellem at indtage en mentorrolle for andre processupportere eller operatører i fabrikken.

I Novo Nordisk baseres beslutninger og handlinger på deres indflydelse på samfundet, miljøet og muligheden for at skabe økonomisk overskud. Det skaber tilsammen en ansvarlig kultur med et sundt og engageret arbejdsmiljø.

Kontakt
Vil du vide mere om stillingen, så kontakt Jeanette Hejli Sørensen på + 45 3075 2412.

Ansøgningsfrist
15. maj 2014

Danmark - Bagsværd Produktion
14-Apr-2014 Administrativ Assistent
Til en nyere etableret afdeling søges en ambitiøs administrativ assistent med reference til afdelingslederen i Biopharm QA New Haemophilia API. Om afdelingen...

Administrativ Assistent

  • Administration
  • Danmark - Gentofte

Til en nyere etableret afdeling søges en ambitiøs administrativ assistent med reference til afdelingslederen i Biopharm QA New Haemophilia API.

Om afdelingen
Vi er en nyere målrettet afdeling med ansvar for kvalitetssikring af FXIII, FVIII og FIX. Du skal have lyst til at arbejde i en QA afdeling, hvor trivsel, høje ambitioner og vedvarende forbedringstiltag er i fokus.

Afdelingen er placeret i både Gentofte og Hillerød.

Jobbet
Du er ledelsens højre hånd og yder højt kvalificeret support og sikrer en velfungerende infrastruktur i afdelingen. Du skal kunne lide at arbejde selvstændigt og synes om at løse praktiske opgaver, der letter hverdagen for andre. Du ser ofte selv, hvor du kan gøre en forskel og tager initiativet til dette. Der vil derfor være gode muligheder for at sætte dit eget præg på stillingens indhold.

Stillingen består overordnet i at udføre administrative opgaver. Udfordringen er at sikre, at alle afdelingernes administrative processer altid er ”up to date”. Dette omfatter dels en række faste administrative opgaver såsom vedligehold af afdelingsmappe og GlobeShare, afregning i Concur og ICE og budgetopfølgning. Endvidere vil der være praktiske opgaver såsom indkøb, opfølgning på afdelingsmål, planlægning af møder samt fx opgaver i forbindelse med personaleansættelser og fratrædelser. Desuden vil du deltage i planlægning og afvikling af den praktiske side af myndighedsinspektioner i Biopharm.

Du er med til at sikre gode samarbejdsrelationer. Bl.a. er samarbejdet med de øvrige QA afdelinger vigtig og der vil også være opgaver på tværs i Biopharm QA området. Du skal derfor have lyst og evne til at kommunikere, være fleksibel og initiativrig. Du vil være en aktiv deltager i netværket for de administrative i Biopharm QA.

Arbejdet foregår i et afslappet og uformelt miljø, hvor vi lægger vægt på trivsel, vilje til at gøre en forskel, humor og engagement.

Kvalifikationer
Du har en relevant administrativ uddannelse og gerne flere års erfaring. Du har allerede demonstreret overbevisende resultater og en ambitiøs tilgang til dit arbejde. Du er rutineret bruger af diverse IT systemer. Dine opgaver kræver både selvstændighed og evne til at kommunikere, og du skal have gode formuleringsevner i både skrift og tale. Som person er du engageret og struktureret med et positivt livssyn og trives som supporter med mange udfordringer.

I Novo Nordisk stræber vi efter at være de bedste. Vi er førende i verden indenfor diabetesbehandling og en større spiller indenfor behandling af blødninger, behandling med væksthormon og behandling med hormonterapi. Derfor kan vi tilbyde vores medarbejdere mulighed for en stærk professionel udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt på Lars Nyholm + 45 3075 5226.

Ansøgningsfrist
21. april 2014

Danmark - Gentofte Administration
14-Apr-2014 Kemiker
Kan du hjælpe os med at etablere og drive en moderne og professionel fyldefabrik? Så kan du blive en del af Novo Nordisk’s største investering i Danmark i mange år. Vi ser frem til at invitere dig ind i en proj...

Kemiker

  • Produktion
  • Danmark - Kalundborg

Kan du hjælpe os med at etablere og drive en moderne og professionel fyldefabrik? Så kan du blive en del af Novo Nordisk’s største investering i Danmark i mange år. Vi ser frem til at invitere dig ind i en projektorganisation, der består af fagligt dygtige, ambitiøse og målrettede medarbejdere.

Om afdelingen
I Biopharm-divisionen af Novo Nordisk har vi blandt andet ansvaret for at producere NovoSeven®, de kommende generationer af hæmofili-præparater, Glucagon og andre Biopharm produkter. Vi oplever en stigende efterspørgsel og har valgt at etablere en ny fabrik i Kalundborg for at sikre fyldning af vores produkter.

Afdelingen kommer til at bestå af lidt over 100 medarbejdere, som over de næste par år skal oplæres og trænes i vask og sterilisation, formulering, fyldning, frysetørring og inspektion af biofarmaceutiske produkter.

Jobbet
I jobbet som Fylde kemiker vil du komme til at samarbejde tæt med operatører, supportere og QA. Hovedvægten i projektfasen vil være at deltage i kvalificeringen af udstyret og processen, samt at sikre en glidende overgang fra projekt til produktion.Når der opstår udfordringer i vores projekt/produktion, er det dig, der sikrer overblikket, så problemerne kan løses hurtigt og effektivt.Deltagelse i større og mindre optimerings- og standardiseringsprojekter bliver også en del af din nye hverdag, samt deltagelse ved myndighedsinspektioner. Derudover deltager du aktivt i at yde daglig support til driften af vores aseptiske produktion. Du spiller således en nøglerolle i arbejdet med at sikre drift og frigivelse af produkterne – og så sikrer du, at afdelingen altid er i compliance med gældende lovkrav.

Kvalifikationer
Du er farmaceut, kemiingeniør eller lignende og har lyst til at udvikle dig i et farmaceutisk produktionsmiljø. Kendskab til mikrobiologi er et stort plus. Du har erfaring fra arbejdet i et GMP-reguleret miljø og forstår, hvad der er god adfærd i en aseptisk produktion. Samtidig kender du til LEAN-værktøjer og er i stand til at bruge det på et højt fagligt niveau.Dine formidlings og kommunikationsevner er i top, og du er en ørn til at samarbejde. Det falder dig også helt naturligt at skabe overblik, selvom du varetager mange forskellige opgaver på samme tid. Samtidig er du resultatorienteret, initiativrig, engageret, fleksibel og vant til at tage ansvar. Sidst, men ikke mindst, har du har en positiv indstilling og lyst til at være en nøgleperson i en stor afdeling. Du taler og skriver både dansk og engelsk flydende.

Site Kalundborg er en by i byen, kun godt en times kørsel fra København. Området er på 1.350.000 m2 med eget vejnet. Vi er 3.500 mennesker i alt fordelt på 16 fabrikker, og vi producerer bl.a. 50 % af verdens insulin. Site Kalundborg kan helt kort sammenfattes til: udviklingsmuligheder uden ende.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Anne-Mette Meldgaard på +45 3075 0190.

Ansøgningsfrist
11. maj 2014

Danmark - Kalundborg Produktion
14-Apr-2014 Laborant
Har du lyst til at arbejde med karakterisering og HPLC i en spændende afdeling, som forestår og behersker en bred vifte af analytiske teknikker, så er dette job utvivlsomt noget for dig. Om afdelingen...

Laborant

  • Forskning og Udvikling
  • Danmark - Måløv

Har du lyst til at arbejde med karakterisering og HPLC i en spændende afdeling, som forestår og behersker en bred vifte af analytiske teknikker, så er dette job utvivlsomt noget for dig.

Om afdelingen
CMC Analytical Support er en afdeling med 67 medarbejdere dedikeret til analyse af Novo Nordisks portefølje af både diabetes og biofarmaceutiske proteiner i klinisk udvikling. Afdelingen udfører analyse og karakterisering af peptider, proteiner, råvarer og lækstoffer. Afdelingen er en del af CMC Drug Product Development i R&D og bor i moderne laboratorier i Måløv.

Jobbet
Du vil primært arbejde med strukturopklaring af produkter og urenheder ved LC-MS (og evt. NMR) samt peptid mapping ved HPLC/UHPLC. I stillingen kommer du til arbejde med udvikling og validering af analysemetoder samt frigivelsesanalyser. Det meste af din tid vil du bruge i laboratoriet, men du vil også være ansvarlig for databehandling og afrapportering af de opnåede resultater. Du vil arbejde tæt sammen med både kemikere og andre laboranter på tværs af Novo Nordisks projekt portefølje. Herudover vil du deltage i øvrige laboratorieopgaver, som f.eks. vedligeholdelse inkl. kvalificering af udstyr samt udarbejdelse af instruktioner.

Da vi arbejder under GMP, er en omhyggelig dokumentation en selvfølge.

Vi optimerer løbende vores arbejdsprocesser via LEAN og du forventes at være engageret i arbejdet med problemløsning og optimeringer sammen med dine kollegaer. Sproget i det daglige er dansk, men vi forventer at du kan både skrive og læse engelsk på teknisk/fagligt niveau.

Kvalifikationer
Du har en uddannelse som laborant eller lignende. Du har mindst 2-3 års solid erfaring inden for strukturopklaring af peptider/proteiner ved LC-MS (f.eks. Orbitrap og Synapt) og MALDI. Du har erfaring med HPLC/UHPLC og gerne peptid mapping. Du er kvalitetsbevidst og har gerne GMP erfaring. Du kan arbejde selvstændigt og kan lide at tage ansvar for analyser og udstyr. Du skal kunne veksle mellem at arbejde på flere forskellige projekter med fokus på selve analysen fra prøveforberedelse til afrapportering af resultatet. Du skal udvise fleksibilitet i en hverdag, hvor opgaverne hurtigt kan blive omprioriteret i overensstemmelse med teamet. Du har en god struktureret tilgang til arbejdet og har lyst til at arbejde sammen med flere forskellige kemikere. Det er yderligere en fordel, at have erfaring med andre teknikker som NMR, sekventering, og gelelektroforese samt erfaring fra pharmaceutisk industri.

I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her handler ikke bare om at tjene til føden, men om at gøre en forskel.

Kontakt
Vil du vide mere om stillingen, så kontakt Marianne Olsen på + 45 3079 2650 eller Camilla Schmidt på + 45 3079 5479

Ansøgningsfrist
25. april 2014

Danmark - Måløv Forskning og Udvikling
14-Apr-2014 Senior QA med et projektorienteret fokus
Vil du være en del af et projektorienteret QA miljø, og have ansvar for kvaliteten i flere af vore store strategiske projekter? Er du klar til en ekspertrolle med markant ansvar, hvor du aldrig går på kompromis...

Senior QA med et projektorienteret fokus

  • Kvalitetssikring
  • Danmark - Kalundborg

Vil du være en del af et projektorienteret QA miljø, og have ansvar for kvaliteten i flere af vore store strategiske projekter? Er du klar til en ekspertrolle med markant ansvar, hvor du aldrig går på kompromis med kvalitet og compliance til gavn for kolleger og patienter over hele verden? Så grib chancen og søg jobbet som QA i Novo Nordisk´s største færdigvarefabrik i Kalundborg.

Om afdelingen
Du bliver en del af QA for Site Danmark (SDK) i Kalundborg, hvor vi tæller 40 dedikerede og engagerede medarbejdere som er fordelt på tre teams – et der varetager QA for aseptisk produktion, hvor vi skal udvide med en fyldelinje og to der varetager QA for montage- og pakke processer samt projekter. Sammen med 9 engagerede kolleger udgør du afdelingens QA med ansvar for kvaliteten i strategisk vigtige projekter både i produktion, IT og lager. Der bliver arbejdet i højt tempo med konstant fokus på compliance og kvalitet. Dette sker i tæt samarbejde med både interne og eksterne projektledere i SDK.

Jobbet
Du får rollen som den afgørende QA person, der med din høje faglighed og kvalitetsviden er med til at bygge kvalitet ind i processerne og udstyret. Du vil deltage i projekter – både store og små – hvor du igennem din viden og kompetencer skal tilsikre, at systemer og processer er i compliance med GMP reglerne. Du får en central rolle og vil skulle træffe afgørende beslutninger, når projekterne skal planlægges og gennemføres.

Foruden opgaver og udfordringer i de projekter, som du er QA på, vil du samtidig være ansvarlig for at QA godkende CR-sager, kvalificeringer, SOP’er og afvigelser relateret til den daglige drift. Du vil blive involveret i problemløsninger i samarbejde med produktionen.

Nogle af de store projekter du skal lykkes med er bl.a.: Revalidering af produktionslinjer, hvor alle montage og pakke linjer skal revalideres. Dette projekt løber i flere år og vil give dig god indsigt i validering. Desuden har vi grundet nye krav om stregkoder på produkter igangsat Serialiseringsprojektet, som varer til 2017. Og i år, på den kortere bane, er vi igang med etablering af ny fyldelinje i aseptisk område. Ved hver implementering skal vi igennem hele valideringsforløbet – fra A-Z.

Kvalifikationer
Du er uddannet farmaceut, ingeniør eller relevant cand.scient uddannelse, og dit cv afspejler minimum 4 års erfaring indenfor QA og/eller GMP produktion, hvor du har fået et bredt kendskab til GMP og farmaceutisk produktion. Derudover skal du kunne kommunikere på både dansk og engelsk – mundtligt så vel som skriftligt.

Vi kan tilbyde et job hvor du er den der samler trådene og udstikker kursen for dine samarbejdspartnere. Du får selvstændigt ansvar for at træffe de afgørende beslutninger. Vi tilbyder et positivt arbejdsmiljø med et ønske og vilje til at løse udfordringer og vi har en åben og ærlig dialog, som foregår i øjenhøjde med hinanden. Du deler gerne ud af dine gode råd og faglige argumenter.

Arbejdsdagene vil være alsidige – ikke to dage er ens, hvilket kræver høj grad af struktur, effektivitet og godt humør.

Du kan lære mere om Novo Nordisk Product Supply og arbejdet i QA ved at bruge linket www.novonordisk.com/careers/QA

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Jytte Holm Iversen på +45 3079 7767.

Ansøgningsfrist
27. april 2014

Danmark - Kalundborg Kvalitetssikring
12-Apr-2014 Håndværker søges til færdigvareproduktion
Vil du proaktivt sikre leveringen af produkter til vores kunder? Kan du trives i et miljø, hvor der er fokus på høj udnyttelse af ressourcer og udstyr? Er du kvalitetsbevidst, omhyggelig og en velanset kollega,...

Håndværker søges til færdigvareproduktion

  • Produktion
  • Danmark - Gentofte

Vil du proaktivt sikre leveringen af produkter til vores kunder? Kan du trives i et miljø, hvor der er fokus på høj udnyttelse af ressourcer og udstyr? Er du kvalitetsbevidst, omhyggelig og en velanset kollega, der vil være med til at skabe en god dialog såvel i dit team som i resten af afdelingen? Så er du måske den nye engagerede medarbejder, vi søger i Biopharm Tablets & Finished Products – Gentofte.

Om afdelingen
Vi er en afdeling på 100 medarbejdere, der er ansvarlige for færdigvareproduktion og shipping af forskellige biofarmaceutiske produkter til kunder i hele verden. Afdelingen er opdelt i 6 teams, hvor du vil blive ny kollega i Team Teknik, som består af 8 håndværkere og 1 teamleder.

Jobbet
I samarbejde med produktionen, processupport og dine øvrige kollegaer i Team Teknik, bliver du ansvarlig for udførelse af planlagte og afhjælpende vedligehold samt udbedring af fejl på afdelingens udstyr. Teamet er ligeledes med til at sikre de løbende forbedringer på udstyret og yder teknisk sparring til afdelingens dygtige ingeniører, når der skal købes og indkøres nye maskiner.

Pakkeriet er sidste led i produktionskæden, og teamet spiller derfor - gennem sikring af stabil drift - en vigtig rolle i optimeringen af kapacitet og leveringsevne.

I Team Teknik arbejder vi primært på fuld- og semiautomatiske pakkemaskiner samt etiketteringsmaskiner. Vi arbejder på 3-holds skift, og er dermed til stede, når der køres produktion.

Stillingen er kategoriseret som F3.

Kvalifikationer
Du er uddannet automatikmekaniker, elektriker eller lignende og har erfaring med vedligehold af procesudstyr. Du skal være bekendt med at arbejde efter skriftlige procedurer og have god forståelse for kvalitet og GMP. Du skal ligeledes være god til at sætte dig ind i tekniske problemstillinger.

Det vil være en fordel, hvis du har bred erfaring med automatik og systematisk problemløsning samt kender til SAP PM, som bruges til styring af vores vedligehold. Du er fortrolig med MS Office og kan dokumentere dine opgaver.

Du får en omskiftelig hverdag, hvor der løbende sker omprioriteringer, og det er derfor en forudsætning, at du er fleksibel og omstillingsparat. I teamet er der en stor grad af ansvar og selvstændighed både i forhold til løsninger og planlægning, og du skal derfor være god til at arbejde både selvstændigt og i team.

I Novo Nordisk kan du få muligheden for at arbejde sammen med dygtige kolleger, som alle har kvalitet og patienten i fokus. Det er dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig en hverdag med talentfulde kolleger samt forskellige muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, kan du fra den 14. april kontakte Henrik Byron på + 45 3079 9078

Ansøgningsfrist
18. april 2014

Danmark - Gentofte Produktion
11-Apr-2014 Automatik Specialist med højt drive og godt humør
Har du stor viden om drift af automatik systemer i et GMP-miljø? Og har du erfaring fra den farmaceutiske verden eller lignende reguleret industri? Vi søger en højt kvalificeret akademisk / teknisk profil med g...

Automatik Specialist med højt drive og godt humør

  • Produktion
  • Danmark - Kalundborg

Har du stor viden om drift af automatik systemer i et GMP-miljø? Og har du erfaring fra den farmaceutiske verden eller lignende reguleret industri? Vi søger en højt kvalificeret akademisk / teknisk profil med gode samarbejdsevner, der trives med at arbejde både operationelt og projektorienteret.

Om afdelingen
Biopharm AP’s fyldefabrik i Kalundborg er en ny aseptisk påfyldnings facilitet, der er ansvarlig for at formulering og fyldning af NovoSeven®, Glukagon® og andre biofarmaceutiske produkter.

IT & Automatik teamet er ansvarlig for drift og vedligeholdelse af facilitetens IT & Automatik udstyr, der dækker kontrolsystemer til formulering, påfyldning, frysetørring, capping og støtte processer. Vi er kendetegnet ved, at vi kender og tager vare på hinanden, og dermed bliver man som ny medarbejder meget hurtigt en del af fællesskabet. Vi lægger meget vægt på engagement, ansvarlighed, respekt og samarbejde samt en positiv, humoristisk omgangstone.

Jobbet
Vi er på udkig efter et nyt medlem til teamet, der kan spille en central rolle i at sikre den rette grad af compliance i de resterende valideringer, driftsfasen og i fremtidige projektvalideringer. Du vil sikkert også drive automatik relaterede opgraderings og forbedringsprojekter.

Vi arbejder primært med teknologierne Proficy iFix, Proficy Historian, PAS -X, Siemens S7 PLC og Siemens WinCC Flexible. Alle automationssystemer er tilsluttet vores fælles procesnetværk. iFix programmering vil også være en del af dit job, specielt i forbindelse med optimering og forbedring af vores SCADA systemer.

Du vil medvirke til at sikre, at vi opererer og validerer vores automatikudstyr, i overensstemmelse med eksterne myndigheders og interne Novo Nordisks krav. Du vil ligeledes støtte dine teamkollegaer i denne proces.

Kvalifikationer
Først og fremmest er du en team-player, og du brænder for at udvikle dit speciale og lære nye ting. Du har et godt humør og en struktureret tilgang til at løse udfordringer på en systematisk, enkel og effektiv måde.

Du har gode kommunikationsevner, både skriftligt og mundtligt, og du kan kommunikere teknisk komplekse informationer til ikke-tekniske kolleger.

Du har sikkert en ingeniør eller lignende akademisk baggrund, med mindst 3 til 5 års erfaring. Det er et krav at du har erfaring med iFix og Historian, samt Computer-System-Validation i et GMP reguleret miljø.Har du derudover erfaring med GAMP og 21 CFR Part 11, er det en yderligere fordel.

Du er en engageret, struktureret, kvalitetsbevidst person, der tager ansvar for både din egen og afdelingens opgaver. Du trives i et arbejdsmiljø hvor ændringer kan ske hurtigt, og du formår at holde fokus eller ændre kurs alt efter hvad der kræves. Du stortrives i en rolle, hvor du kan udfolde din faglige viden og bringe din argumenter og forhandlingsevner i spil. Du byder forandringer velkommen og udfordrer gerne vores måde at gøre tingene på, så vi bliver endnu bedre.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Hvis du ønsker at vide mere om stillingen, så kontakt Anders Engberg på + 45 3079 2628.

Ansøgningsfrist
30. maj 2014

Danmark - Kalundborg Produktion
11-Apr-2014 Laborant
Har du den viden og erfaring der skal til, for at skabe nyt og udvikle fremtidens diabetes produkter? Hvis ja, så har du muligheden for at spille en nøglerolle i CMC Diabetes Formulation Development i Måløv. So...

Laborant

  • Forskning og Udvikling
  • Danmark - Måløv

Har du den viden og erfaring der skal til, for at skabe nyt og udvikle fremtidens diabetes produkter? Hvis ja, så har du muligheden for at spille en nøglerolle i CMC Diabetes Formulation Development i Måløv. Som bindeledet mellem forskning og produktion, er vi ansvarlige for at udvikle subkutane injicerbare formuleringer og processer – hele vejen fra tidlig udvikling til fase III klinikstudier og registrering.

Om afdelingen
Afdeling CMC Diabetes Formulation Development, som er en del af R&D, er organiseret i to teams med i alt 30 personer. Afdelingen repræsenteres i projektgrupper på tværs af organisationen, hvor vi hele tiden bestræber os på at levere resultater af en høj kvalitet. Du vil blive en del af Team Diabetes Formulation Development I som er ansvarlig for formuleringsudvikling og procesudvikling, inklusiv stabilitet og dokumentation til kliniske studier.

Team Diabetes Formulation Development I består af 6 laboranter og 12 kemikere samt en teamleder. Vi er gode kollegaer, som sætter pris på samarbejde og teamwork.

Jobbet
Vi kan tilbyde et spændende og udfordrende arbejdsmiljø, hvor du kan bidrage ved at gøre en forskel. Dine opgaver bliver efter overordnede retningslinjer fra kemiker eller teamleder, selvstændigt at planlægge, fremstille, resultatvurdere og præsentere resultater fra udviklings- og stabilitetsforsøg. Du vil skulle planlægge, forberede og gennemføre præparation af aseptiske formuleringer til formuleringsudviklingsforsøg og stabilitetsstudier. Vi forventer, at du aktivt deltager i tilrettelæggelse af det daglige arbejde i laboratorierne således, at projekternes tidsplaner kan overholdes, samt at du er med til løbende at forbedre vores processer gennem cLEAN.

Kvalifikationer
Laboratorieteknisk basisuddannelse som f.eks. farmakonom, bioanalytiker, laborant eller kemotekniker. Du har praktisk faglig erfaring indenfor områderne proteinkemi og udvikling af sterile, farmaceutiske præparater suppleret med generel viden om GXP og anvendelse af IT software. Erfaring eller interesse for Excel vil være en fordel. Du er teamwork-orienteret med gode evner for samarbejde og du har lyst til at lære nyt. Du er omhyggelig, ferm til at organisere og planlægge dit arbejde, og du kan arbejde selvstændigt og ansvarsfuldt i laboratoriet. Som person er du positiv, fleksibel og har et godt humør.

I Novo Nordisk stræber vi efter at være de bedste. Vi er førende i verden indenfor diabetesbehandling og en større spiller indenfor behandling af blødninger, behandling med væksthormon og behandling med hormonterapi. Derfor kan vi tilbyde vores medarbejdere mulighed for en stærk professionel udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Rozana Sten på + 45 3075 2472.

Ansøgningsfrist
27. april 2014.

Danmark - Måløv Forskning og Udvikling
11-Apr-2014 Kemiker Lab
Har du lyst til at arbejde i et team i vækst med inspirerende kolleger med team spirit? Sætter du din faglighed højt og er omhyggelig med det, du laver? Har du sans for sproglig formulering og synes du også det...

Kemiker Lab

  • Produktion
  • Danmark - Kalundborg

Har du lyst til at arbejde i et team i vækst med inspirerende kolleger med team spirit? Sætter du din faglighed højt og er omhyggelig med det, du laver? Har du sans for sproglig formulering og synes du også det er sjovt at være med i praktisk arbejde i laboratoriet? Så kunne du være præcis den kollega, vi søger i Seed Lab and IPC?

Om afdelingen
Biopharmaceuticals er en del af Novo Nordisks produktion, hvor vi producerer en række af Novo Nordisks produkter. Vi er i alt 1.800 medarbejdere fordelt på flere af Novo Nordisks sites på Sjælland. Du bliver en del af Biopharmaceuticals produktion i Kalundborg, hvor vi producerer den aktive ingrediens i produktet NovoSeven® (hæmofili-præparat). Produktionsprocessen består af mammal celledyrkning med efterfølgende kromatografisk oprensning og vi producerer døgnet rundt, året rundt. Vi udgør i alt ca. 100 medarbejdere på det 3.500 mand store site i Kalundborg.

Jobbet
Seed Lab and IPC er et team på 4 kemikere og 9 laboranter. Vi udfører den første del af opformeringsprocessen i produktionen af NovoSeven®. Vi udfører analyser som overvågning af produktionsprocessen. Vi indgår således i produktionslinjen og er samtidigt et laboratorium. Dette giver en spændende bredde i opgaver og dagligdag. Vi følger skarpt op på driften hver dag, håndterer hændelser, reviewer logbøger og opdaterer SOP’er. Dokumentation og overholdelse af krav og regler er en vigtig brik i arbejdet, som sker i tæt samarbejde med vores QA afdeling. Du vil arbejde tæt sammen med laboranter og øvrige kemikere i teamet, såvel i laboratoriet som ved skrivebordet.

Produktionsdelen udgøres af vores Podelaboratorium, hvor vi under aseptiske forhold opformerer mammale celler fra ampul til produktionstank. Laboratoriedelen omfatter IPC (In Process Control) analyser, pH, celletælling, mikroskopi, glucose, titreringer, ELISA og PCR under kvalificering. I jobbet indgår kvalificering af udstyr og analysemetoder. Vi står overfor at skulle kvalificere både nye nitrogenfrysere og inkubatorer, samt nyt udstyr til ELISA og at skulle indføre PCR og indrette et nyt laboratorium.

Kvalifikationer
Du har en akademisk naturvidenskabelig uddannelse, ingeniør, cand. polyt, cand. scient eller cand. pharm. Du taler og skriver dansk og engelsk på højt niveau. Din erfaring og dit kompetenceniveau afgør omfanget af opgaver og ansvar, hvilket gør det til et udfordrende job, hvad enten du er nyuddannet eller har erfaring. Du kan kombinere højt kvalitetsniveau med overholdelse af deadlines, er omhyggelig og gør dig umage med dit arbejde. Du er fleksibel og tør være åben og ærlig, da det er nøglen til tillid og samarbejde i et team. Du skal kunne fokusere, samtidig med at du har overblik over dine opgaver og deadlines.

Din positive indstilling og dit smittende engagement gør det nemt for dig at samarbejde med kolleger uanset organisatorisk placering.

Novo Nordisk i Kalundborg er en by i byen. Vi er 3.500 mennesker i alt fordelt på 16 fabrikker med en lang række forskellige funktioner, så der er rige muligheder for faglig udvikling.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Trine Wolff på + 45 3075 5032.

Ansøgningsfrist
27. april 2014

Danmark - Kalundborg Produktion
11-Apr-2014 Automatikingeniør
CMC API Development har ca. 350 ansatte. Vi er ansvarlige for API fremstilling og proces-udvikling af nye API kandidater til alle Novo Nordisk udviklingsprodukter. Dette inkluderer områderne gæring, dyrkning, k...

Automatikingeniør

  • Forskning og Udvikling
  • Danmark - Bagsværd

CMC API Development har ca. 350 ansatte. Vi er ansvarlige for API fremstilling og proces-udvikling af nye API kandidater til alle Novo Nordisk udviklingsprodukter. Dette inkluderer områderne gæring, dyrkning, kemisk syntese, grovrens og finrens. Der er stor fokus på en stabil produktion og altid et stort antal spændende projekter i pipelinen. Vi søger derfor en dygtig automatikingeniør, som har lyst til at beskæftige sig med drift og kvalificering af proceskontrolsystemer samt deltagelse på større og mindre investerings-projekter.

Om afdelingen
Vi er en teknisk supportafdeling og vores primære opgaver er at supportere og sikre en stabil drift. Vi er ca. 45 personer og dækker over mange faggrupper herunder: projektledelse, automatik, vedligehold, kalibrering, SAP og drift af forsyningsanlæg. I teamet Technical Compliance and Automation løser vi en lang række opgaver i forbindelse med drift og vedligehold af automatik-systemer samt projektkoordinering af mindre anlægsopgaver.

Jobbet
Du bliver en del af et team på 9 engagerede ildsjæle, som er dedikerede til at supportere vores kunder på tværs af alle pilotanlæg i Bagsværd. Din opgave er overordnet support på automatik, hvor vi har SattLine og DeltaV som PCS systemer. Jobbet indebærer sikring af at styresystemerne er i compliance med gældende regler, håndtering af daglig support samt trouble shooting i kontrolrummet. Du vil gennemføre ændrings- og kvalificeringsopgaver i samarbejde med vores kunder i piloterne.

Som person er du god til at holde styr på dine opgaver og du arbejder selvstændigt. Du er selvsikker og er i stand til at sætte dig igennem og få indflydelse. Dine stærke kommunikative kompetencer gør dig til en troværdig og overbevisende kommunikator.

Du formår at sprede entusiasme og energi omkring dig, og du besidder stærke networking og relationelle kompetencer.

Vi er en organisation som løbende har behov for at udvikle nye ledere, derfor vil ambitioner om ledelse være at en fordel.

Du kommer helt sikkert ikke til at kede dig og kan se frem til en afvekslende hverdag i samarbejdet med vores kunder på tværs af organisationen samt med vores eksterne leverandører.

Kvalifikationer
Du har gennemført en akademisk uddannelse og har erfaring samt en stærk interesse for automatik. Vi er underlagt store kvalitetskrav, så forståelse og kendskab til GMP, GAMP, ISA95/88 er et plus. Høj disciplin omkring opgaveudførelse og grundig dokumentation af alt udført arbejde er et krav. Vi lægger vægt på, at du har et godt humør og kan lide at tage fat i opgaverne, også når de ikke bliver lagt tilrette foran dig.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med mange gode kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Andreas Heuer på + 45 3079 8595.

Ansøgningsfrist
30. april 2014

Danmark - Bagsværd Forskning og Udvikling
11-Apr-2014 Processupporter til Victoza
Novo Nordisk skaber fortsat stor vækst og gode resultater. Derfor har vi brug for en processupporter med højt energiniveau og lederambitioner til vores Purification Plant i Kalundborg. Med udgangspunkt i din vi...

Processupporter til Victoza

  • Produktion
  • Danmark - Kalundborg

Novo Nordisk skaber fortsat stor vækst og gode resultater. Derfor har vi brug for en processupporter med højt energiniveau og lederambitioner til vores Purification Plant i Kalundborg. Med udgangspunkt i din videregående uddannelse, din viden om kemi og din sans for kvalitet, får du en vigtig rolle i vores arbejde med at understøtte produktionen.

Din nye arbejdsplads er Novo Nordisks produktions-site i Kalundborg. Vi er 2.600 kolleger, der bl.a. producerer 50 % af verdens insulin. Du kan glæde dig til at blive del af en organisation, der altid stræber højere. Alle medarbejdere har naturligvis personlige udviklingsplaner, og vi har sat vores videndeling i system i formaliserede faglige netværk.

Om afdelingen
Dit nye arbejde handler om finrensning af det nye og spændende produkt Victoza i afdelingen PPIII. Du bliver en del af et team på 18 akademikere og teknikere. Vi har ansvaret for processer og udstyr. Det drejer sig bl.a. om kromatografiske søjler, fældning, centrifugering, organisk syntese og råvare/solvent blanderi.

Jobbet
I dette job vil du primært skulle arbejde med vores råvare solvent afsnit, som er et område under stor udvikling, og du vil derfor få mulighed for at forme og sætte retning for denne slags processer fremadrettet. Du supporterer operatørerne i driften og træffer hurtigt beslutninger, hvis der opstår uforudsete driftsstop eller afvigelser – og efterfølgende identificerer du årsagen, ved at bruge systematisk problemløsning og lean-værktøjer. Daglig rapportering og dokumentation er derfor også meget vigtige ingredienser i dit nye job. Herunder håndterer du store datamængder, som du forvandler til forståelige procesbeskrivelser, der viser sammenhænge mellem data og processer.

Kvalifikationer
Kemisk viden og forståelse af processer og udstyr. Du har en videregående kemisk orienteret uddannelse (fx kemi ingeniør), som gør, at du er god til kemi og forstår sammenhængen mellem processer og udstyr. Der er GMP i alt, hvad vi laver, så forståelse og kendskab til dette er et stort plus. Samtidig er du skarp på rapportering og dokumentation, og i den sammenhæng er det vigtigt du kan lide at behandle og se på data. Derudover er det vigtigt, at du trives i en hverdag med højt tempo, hvor du har rigtigt mange kontakter på alle niveauer og på tværs af faggrupper. Da tæt samarbejde er en grundlæggende forudsætning for vores succes, skal du også være udpræget team-player. Vi har en forventning om du bor inden for en rimelig afstand af Kalundborg eller være villig til at flytte.

Gør dig synlig til et fremtidigt job i produktionen: Vi har løbende nye stillinger inden for processupport. Så er der ikke en stilling, der rammer plet lige nu, så giv din interesse til kende ved at lave en uopfordret ansøgning via novonordisk.com/UA.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så er du meget velkommen til at kontakte Kim Ejlersen på + 45 3075 1099.

Ansøgningsfrist
25. april 2014

Danmark - Kalundborg Produktion
11-Apr-2014 Laborant til Protein Test Maskinen
Vi søger fagligt stærke laboranter som trives med at arbejde med mange forskellige teknologier inden for rekombinant protein produktion til en afdeling under Protein Chemistry området. Om afdelingen...

Laborant til Protein Test Maskinen

  • Forskning og Udvikling
  • Danmark - Måløv

Vi søger fagligt stærke laboranter som trives med at arbejde med mange forskellige teknologier inden for rekombinant protein produktion til en afdeling under Protein Chemistry området.

Om afdelingen
Protein Chemistry området består af 20 forskningskemikere og 25 laboranter fordelt på tre forskellige forskningsenheder. Protein Chemistry er en del af Diabetes Protein Engineering funktionen i Diabetes Research Unit (DRU) og er involveret i den tidlige fase af frembringelsen af nye terapeutiske proteinkandidater til behandling af diabetes og fedme. Vore medarbejdere arbejder primært inden for vores ekspertiseområder som er proteinoprensning, analyseudvikling og karakterisering.

Protein Test Maskinen er en afdeling på 15 personer, som udgør en yderst vigtig basis for at supportere den tidlige R&D pipeline for Novo Nordisk. Formålet er løbende at kunne levere et højt antal færdigoprensede rekombinante proteiner til de første analyser af proteinernes biologiske og terapeutiske potentiale. Leveringen af proteiner foregår på basis af en high-throughput teknologisk platform som er det centrale omdrejningspunkt for afdelingen. Proteinerne vil blive delvist karakteriseret for at sikre høj kvalitet.

En stor ekspertise indenfor rekombinant ekspression og proteinoprensning er nødvendig for at kunne levere proteinerne og afdelingen benytter sig af adskillige teknologier inden for både protein kemi og molekylær biologi. Protein Test Maskinen har en meget stor berøringsflade med hele forskningsorganisationen, da den samarbejder med flere forskningsprojekter og grupper både i Novo Nordisk DK og Novo Nordisk Beijing.

Jobbet
Du vil primært komme til at arbejde med protein oprensning teknikker. Du vil arbejde med etablering og kørsler af nye oprensningsscreeninger og oprensningsprocedurer ved brug af state-of-the-art oprensnings teknologi. Endvidere omfatter arbejdet UPLC/HPLC kørsler, anvendelse af eletroforetiske metoder, MS analyse og stabilitets studier af de oprensede proteiner. Erfaring inden for ekspression af proteiner i mammale cellelinjer eller mikrobielle organismer betragtes som en fordel. Du forventes at bidrage til løbende optimering af disse discipliner og på baggrund af din store praktiske erfaring deltage aktivt i den videre udvikling af afdelingen.

Kvalifikationer
Du har en solid baggrund og ekspertise indenfor proteinoprensning og anvendelse af FPLC systemer (ÄKTA) samt proteinhåndtering og analyse. Du har ligeledes kendskab til metoder indenfor rekombinant protein ekspression. Du trives godt med at levere til deadlines, er omstillingsparat i forhold til dit job, tager gerne imod nye teknologiske udfordringer og arbejder selvstændigt. Du har ordenssans og er vant til løbende at optimere dine arbejdsgange, så de bliver endnu bedre. PC kendskab er en fordel og god praksis for data dokumentation er påkrævet. Som person er du positiv, fleksibel og har et godt humør.

Du er udadvendt og er god til at arbejde sammen med dine kollegaer.

I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her handler ikke bare om at tjene til føden, men om at gøre en forskel

Kontakt
Vil du vide mere om stillingen, så kontakt Allan Shaw på + 45 3079 4403.

Ansøgningsfrist
30. april 2014.

Danmark - Måløv Forskning og Udvikling
10-Apr-2014 Laborant til Bioanalyse med Aktivitets- og Immunoassays
Har du lyst til at arbejde som laborant med udvikling og validering af bioanalytiske metoder samt rutineanalyse af prøver? Om afdelingen...

Laborant til Bioanalyse med Aktivitets- og Immunoassays

  • Forskning og Udvikling
  • Danmark - Måløv

Har du lyst til at arbejde som laborant med udvikling og validering af bioanalytiske metoder samt rutineanalyse af prøver?

Om afdelingen
I Development Bioanalysis arbejdes der med forskellige bioanalytiske metoder til måling af lægemiddelkandidater i blodprøver fra både non-kliniske og kliniske studier. Afdelingen beskæftiger 48 personer, hvoraf 25 er laboranter eller bioanalytikere.

Jobbet
Development Bioanalysis søger en laborant eller bioanalytiker til arbejde med immuno- og aktivitetsassays indenfor hæmofili.

Vi er en afdeling, som står overfor mange udfordrende og spændende opgaver, der stiller store krav til gode samarbejdsevner og forandringsparathed. Vi arbejder gerne med systematisk problemløsning og løbende forbedringer af vores arbejde. I stillingen kommer du til at arbejde med metodeudvikling og validering af analysemetoder som chromogene og clot assays, ELISA og AlphaLISA, samt rutineanalyse af blodprøver fra diverse studier under GLP eller GCP.

Kvalifikationer
Vi søger en engageret laborant eller bioanalytiker, som drives af nye udfordringer og varieret arbejde i et travlt, men spændende og positivt arbejdsmiljø. Som person skal du være omhyggelig, have drivkraft, være fleksibel og initiativrig samt have sans for kvalitet. Erfaring med immunoassays/ELISA og GLP eller andre kvalitetssikringssystemer samt kendskab til chromogene og/eller clot assays vil være en fordel. Fremtiden byder på store udfordringer i laboratoriet, derfor skal du være klar til forandringer og til at bidrage med forslag til at forbedre arbejdsgange og metoder. Vi benytter et LIMS system til alt fra registrering af prøver til planlægning af analysearbejde samt beregning af data. Interesse for at arbejde med IT systemer samt erfaring med Windows Office pakken er derfor nødvendig. Teamets officielle sprog er engelsk og det er derfor et yderligere krav, at du har lyst til at begå dig på engelsk.

Du vil indgå i et team af laboranter og kemikere, som har en munter, omhyggelig, effektiv og gensidig hjælpsom tilgang til arbejdet. Derfor er et godt humør, gode samarbejdsevner og en struktureret arbejdsform en selvfølge. Du er desuden fleksibel og arbejder ligeså godt selvstændigt som i teams. Der er masser af muligheder for at udvikle både personlige og faglige kompetencer for den rette engagerede person.

I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her handler ikke bare om at tjene til føden, men om at gøre en forskel.

Kontakt
Vil du vide mere om stillingen, så kontakt Thomas Krogh-Meibom på telefon + 45 3075 6133 eller Tine R. Poulsen på + 45 3075 5323.

Deadline
23. april 2014.

Danmark - Måløv Forskning og Udvikling
10-Apr-2014 Kemiker
Vil du arbejde med verdensklasse produktion af Novo Nordisks montage og pakning af insulinprodukter i Kalundborg. Og er du klar til et markant ansvar med fokus på kvalitet, produktion og processer samt faglig o...

Kemiker

  • Produktion
  • Danmark - Kalundborg

Vil du arbejde med verdensklasse produktion af Novo Nordisks montage og pakning af insulinprodukter i Kalundborg. Og er du klar til et markant ansvar med fokus på kvalitet, produktion og processer samt faglig og personlig udvikling? Så er du sikkert vores nye kollega i processupporter teamet, der består af 15 højt engagerede medarbejdere? Vi skaber fortsat stor vækst og gode resultater og har derfor brug for en processupporter med højt energiniveau og gerne lederambitioner.

Om afdelingen
Du kommer til at indgår i Prefilled Device Support, Site Ka i Kalundborg. Vi supporterer driften af montage- og pakkelinier, optimerer processer og sikrer udstyrets valideringstilstand, så vi kan holde antallet af afvigelser på et minimum. Vi håndterer ændringer og løser problemer effektivt og i komplet overensstemmelse med gældende krav.

Jobbet
Dit ansvar er at supporter montage- og pakkelinjer i afdelingen Prefilled Device, således at kravene til validering, kvalitet, compliance og GMP er overholdt. Du vil få ansvaret for en konkret produktionslinje, hvor din hverdag byder på tekniske udfordringer og du løser pludseligt opståede problemer i produktionen, også her anvender du LEAN værktøjerne. Du sørger hele tiden for at skabe fremdrift i dine opgaver bl.a. ved at involvere relevante kolleger fra andre områder til opgave- og problemløsning. Du deltager i inspektioner - både eksterne og interne audits.

Din primære kontaktflade er operatører, reparatører og ledere i produktionen samt logistik og QA. Du sikrer din succes ved at holde fokus på dels kvalitet og leadtime på dine opgaver samt sikre en god relation til dine interessenter.

Du trives som en del af et engageret team, hvor vi lægger stor pris på samarbejde og trivsel. Derfor er det helt essentielt, at du er både åben og udadvendt og samtidig har en god portion empati. Teamet står over for en spændende udfordring, som er at skabe stabile processer, samtidig med at kapaciteten øges. Ud over det øges kravet om compliance hele tiden. Området er i det hele taget i en rivende udvikling, hvor vi har mange bolde i luften og mange interessenter at forholde os til.

Kvalifikationer
Du har en videregående uddannelse med et videnskabelig eller teknisk fokus som fx proces- eller produktionsingeniør gerne suppleret med relevant erfaring. Du er dit ansvar bevidst og formår at træffe de nødvendige beslutninger for at løse udfordringer med sans for effektivitet og kvalitet. Du har et godt overblik og en skarp analytisk sans, som gør det nemt for dig at skære ind til benet og gennemskue sammenhænge fx mellem processer, materialer og udstyr.

Er du nyuddannet skal du besidde et stort drive for at lykkes i stillingen, og du skal indstille dig på en stejl læringskurve. Du taler og skriver flydende engelsk og dansk.

I Novo Nordisk baseres beslutninger og handlinger på deres indflydelse på samfundet, miljøet og muligheden for at skabe økonomisk overskud. Det skaber tilsammen en ansvarlig kultur med et sundt og engageret arbejdsmiljø.

Kontakt
Vil du vide mere om stillingen, så kontakt Ole S. Iversen på + 45 3075 2649.

Ansøgningsfrist
5. maj 2014.

Danmark - Kalundborg Produktion
10-Apr-2014 QA tekniker
Kunne du tænke dig at være en del af kvalitetssikringen og kontrollen af glucagon og hæmofiliprodukter i Novo Nordisk A/S? Trives du i situationer der kræver et personligt ansvar og evne til at tage beslutninge...

QA tekniker

  • Kvalitetssikring
  • Danmark - Gentofte

Kunne du tænke dig at være en del af kvalitetssikringen og kontrollen af glucagon og hæmofiliprodukter i Novo Nordisk A/S? Trives du i situationer der kræver et personligt ansvar og evne til at tage beslutninger med kvaliteten i fokus?

I Biopharm QA sikrer vi kvalitet ved at være tæt på processen og ved at kontrollere stikprøver af de producerede enheder. Vi søger derfor en engageret QA medarbejder der har lyst til at være med til at tage det ansvar.

Om afdelingen
Biopharm QA AP er ansvarlig for kvalitetssikring af 3 aseptiske fyldefabrikker samt forsyninger til Site Ge. Den ledige stilling er i team 545.06 QA-Visuel Inspektion, som arbejder med kvalitetssikring og kontrol af stikprøver fra to fyldeafdelinger beliggende i Gentofte.

Den ene fyldeafdeling producerer markedsførte hæmofiliprodukter, glucagon og solvenser og desuden nye produkter til klinikproduktion. Den anden fyldeafdeling producerer glucagon til markedet.

Vi kan tilbyde et job blandt dygtige kollegaer i et område, hvor du vil få et godt overblik over myndighedsforventninger og krav i den farmaceutiske industri.

Jobbet
Som QA tekniker i team QA-Visuel Inspektion vil din hverdag primært være inde i produktionsområdet. Her vil du være ansvarlig for at udføre visuel inspektion af stikprøver på fyldte glasenheder og du vil være ansvarlig for det tilhørende papirarbejde. Derudover består arbejdsopgaverne af QA review af logbøger samt stempling og udlevering af batchdokumentation til produktionerne.

Du bidrager via dit arbejde til at kvalitetssikre og kvalitetskontrollere det produkt der frigives og du er med til at sikre det rette quality mindset og GMP-niveau i fyldeafdelingerne.

Kvalifikationer
Du har en uddannelse som laborant, farmakonom eller tilsvarende. Erfaring fra GMP produktion eller analyselaboratorier er at foretrække, men er ikke en forudsætning for at komme i betragtning. Du skal kunne trives med at jobbet i høj grad består af praktisk arbejde, der udføres sammen med dine QA kollegaer ude i fyldeafdelingerne.

Du besidder evnen til at foretage selvstændige vurderinger, men også evnen til at spørge efter hjælp når du er i tvivl. Du skal have et quality mindset, som sikrer at du altid sætter kvalitet først.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Rasmus Madelung Nielsen på + 45 3075 6071.

Ansøgningsfrist
23. april 2014

Danmark - Gentofte Kvalitetssikring
10-Apr-2014 Specialist drømmejob i QA til større projekter
Vil du være med til at præge og sætte faglig retning for en afdeling i rivende udvikling og vækst? Brænder du for at gøre en forskel og forbedre mange menneskers liv ved at sikre kvaliteten af insulinproduktion...

Specialist drømmejob i QA til større projekter

  • Kvalitetssikring
  • Danmark - Kalundborg

Vil du være med til at præge og sætte faglig retning for en afdeling i rivende udvikling og vækst? Brænder du for at gøre en forskel og forbedre mange menneskers liv ved at sikre kvaliteten af insulinproduktionen i Product Supply? Har du solid erfaring med QA og ønsker du at gå specialistvejen ved at prøve kræfter med større kvalificering- og valideringsprojekter? Så er du måske den rette person til jobbet som Senior QA Kemiker til QA for Insulin Manufacturing II i Kalundborg, verdens største insulinproduktion.

Om afdelingen
QA for Insulin Manufacturing II er en afdeling i rivende udvikling med pt. 35 engagerede og motiverede medarbejdere fordelt på 3 teams. Vi er ansvarlige for Novo Nordisks produktion af human insulin API, lige fra gæring til finrensning.

Vores fornemmeste opgave er at yde kvalitets support til alle aktiviteter i produktionen både til daglig drift og større projekter. Du vil blive en del af teamet med de mest erfarne QA medarbejdere, der er med til at drive de store strategiske projekter inden for QA.

Jobbet
Dit overordnede ansvar er at sætte retning for kvalitet og compliance ud fra de myndighedskrav, vi efterlever. Det gør du ved at udfordre og godkende forslag og løsninger samt coache produktionen til at levere i den rette kvalitet.

Som senior QA medarbejder bliver du afdelingens orakel, der har svar på alle detaljer i forbindelse med GMP. Dit job bliver f.eks. at sagsbehandle validerings- og kvalificeringsdokumentation samt løbende at vurdere compliance-niveauet og identificere og prioritere eventuelle gaps. Som den erfarne QA kemiker får du en særlig opgave i at drive og lede større projekter indenfor blandt andet kvalificering og validering.

Du vil få mange faglige udfordringer i en meget varierende hverdag, hvor ikke to dage er ens. I tilfælde af komplicerede afvigelser er det dig, der er med til at sætte retning for, hvordan de løses. Du får en stor kontaktflade til produktionens afdelinger, og det er derfor væsentligt, at dine kommunikative evner er stærke, og at du kan samarbejde på tværs i organisationen.

Kvalifikationer
Du har en akademisk uddannelse som fx cand.scient, ingeniør, pharmaceut eller dyrlæge kombineret med erfaring fra farmaceutisk produktion. Da vi søger en erfaren senior QA med en stærk faglig profil forestiller vi os, at du har mindst 5 års erfaring med fortolkning af GMP regler indenfor QA, alternativt mindst 7 års erfaring med arbejdet i GMP regulerede miljøer indenfor farmaceutisk produktion eller en viden, der svarer til dette. Med din baggrund inden for GMP ved du, hvordan komplicerede afvigelser skal løses, og hvordan vi får et godt samarbejde både i afdelingen og med vores samarbejdspartnere.

Du beskrives som en person med et godt humør og en åben tilgang til dine omgivelser. Du skal selvstændigt kunne drive processer og med en god energi kunne håndtere udfordringer, også i de mere travle perioder.

Site Kalundborg er en by i byen, kun godt en times kørsel fra København. Området er på 1.350.000 m2 med eget vejnet. Vi er 3.500 medarbejdere i alt fordelt på 16 fabrikker, og vi producerer bl.a. 50 % af verdens insulin. Site Kalundborg kan helt kort sammenfattes til: udviklingsmuligheder uden ende.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Du kan lære mere om Novo Nordisk Product Supply og arbejdet i QA ved at bruge linket www.novonordisk.com/careers/QA

Kontakt
Vil du vide mere om stillingen så kontakt Nanna-Freja Riis Larsen på + 45 3079 1736.

Ansøgningsfrist
28. april 2014

Danmark - Kalundborg Kvalitetssikring
10-Apr-2014 Kvalitetsansvarlig kemiker til nyt pilot plant i Bagsværd
Har du lyst til at tage ejerskab for at sikre kvaliteten i et helt nyt anlæg til oprensning af fremtidens insuliner og GLP-1’er i pilotskala, så er muligheden her. Vi står overfor udfordringen at skulle øge fre...

Kvalitetsansvarlig kemiker til nyt pilot plant i Bagsværd

  • Forskning og Udvikling
  • Danmark - Bagsværd

Har du lyst til at tage ejerskab for at sikre kvaliteten i et helt nyt anlæg til oprensning af fremtidens insuliner og GLP-1’er i pilotskala, så er muligheden her. Vi står overfor udfordringen at skulle øge fremstillingskapaciteten indenfor vores stigende udviklingsportefølje af diabetes produkter. Til den opgave søger vi en dygtig og engageret kemiker.

Om afdelingen
Afdelingen er Downstream Pilot Plants, som hører under området CMC API Development. Afdelingen består af 4 eksisterende pilot plants, der oprenser proteiner til toksikologiske og kliniske studier og et supportteam, der understøtter driften af anlæggene.

Jobbet
Vi tilbyder en spændende stilling som kvalitetsansvarlig kemiker. Du bliver ansvarlig for kvalitets-fagpakken i projektet, hvor du i tæt samarbejde med de øvrige medarbejdere i teamet får til opgave at gennemføre kvalificering iht. GMP-reglerne og bringe det nye pilotanlæg i stabil drift.

Dermed får du en vigtig opgave i at skabe en rød tråd igennem projektforløbet, således at de beslutninger og valg vi træffer undervejs er med til at sikre gode simple løsninger, der i sidste ende betyder stabil drift og compliance med GMP-reglerne. Når anlægget er indkørt og i drift, vil opgavernes art ændre sig til at fokusere på den løbende drift, men stadig med kvalitet og GMP som primært fokus.

Jobbet kræver, at du har tæt samarbejde med de andre i teamet samt vores samarbejdspartnere, herunder det rådgivende ingeniørfirma, QA og teknisk support.

Vi tilbyder et spændende og afvekslende job i et åbent og dynamisk arbejdsmiljø, hvor du vil opleve stor frihed til at løse opgaverne på din måde. Du vil i teamet få en flok engagerede og hjælpsomme kolleger, der ligesom du synes, at det er vigtigt, at det er sjovt at gå på arbejde.

Kvalifikationer
Du har en naturvidenskabelig uddannelse som f.eks. cand. scient. eller ingeniør. Du forventes at tage lederskab for kvalitets-fagpakken – og vores drømmekandidat har tilsvarende erfaring med kvalificering og validering ifm. et større anlægsprojekt i den farmaceutiske branche.

Det er vigtigt, at du det ene øjeblik evner at bevæge dig på konceptuelt niveau ift. de overordnede valideringsprocedurer, for øjeblikket efter at kunne finde en praktisk løsning på eks. en valideringsafvigelse. Det er påkrævet, at du tør tage initiativ til at opsøge viden og at du kan beslutte, hvordan du kommer videre med opgaverne.

Da det rådgivende ingeniørfirma er fra England, skal du være flydende på engelsk.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Thomas Busch på telefon + 45 3079 0533.

Ansøgningsfrist
7. maj 2014.

Danmark - Bagsværd Forskning og Udvikling
10-Apr-2014 Erfaren projektleder til Facility Management
Har du solid erfaring med projektledelse, og kan du sikre rettidig eksekvering af større, komplekse byggeprojekter? Så læs endelig videre. For at kunne gennemføre ændringer på vores bygninger og installatione...

Erfaren projektleder til Facility Management

  • Produktion
  • Danmark - Bagsværd

Har du solid erfaring med projektledelse, og kan du sikre rettidig eksekvering af større, komplekse byggeprojekter? Så læs endelig videre.

For at kunne gennemføre ændringer på vores bygninger og installationer lukker vi den aseptiske produktion i Bagsværd ned to gange om året. Vi har derfor brug for en erfaren projektleder til denne kritiske og tværorganisatoriske opgave.

Om afdelingen
Du bliver en del af Facility, Metrology and Fine Mechanics, hvor vi er 40 kolleger, som arbejder målrettet for at yde support til den aseptiske produktion. Vi sikrer forsyninger af bl.a. vand, damp og ventilation og overvåger at disse er stabile. Vi sikrer, at alt udstyr i produktionen er kalibrereret og at huset fremstår i god stand. Vores værksted fremstiller reservedele og udstyr til den aseptiske produktion.

Jobbet
Som projektleder skal du stå for både planlægning og eksekvering af nedlukningen af vores produktion om sommeren og vinteren. Du skal sikre, at alle arbejder i og på bygningen udføres til tiden, til den aftalte pris og i henhold til gældende retningslinjer for en aseptisk produktion dvs. i henhold til GMP.

Sommer og vinter nedlukning er for os to meget kritiske perioder, hvor vi skal nå at udføre alt det arbejde, vi ikke kan lave mens produktionen kører. Det betyder, at der arbejdes 24/7 i nedlukningsperioden, og at en afgørende succes faktor er, at deadline for genopstart af produktionen overholdes.

Foruden disse to årlige projekter vil du ligeledes blive trænet til rollen som ekspert i vores interne projektledelsessystem, ligesom du skal lede øvrige byggeprojekter. Du vil derfor blive en vigtig spiller i forbindelse med vores samlede projekt portefølje.

Kvalifikationer
Du har en videregående uddannelse, en god teknisk forståelse og sans for kvalitet. Vi lægger vægt på, at du har en dokumenteret og solid projektledererfaring, som du kan have erhvervet fra bygge- og anlægsbranchen eller en farmaceutisk virksomhed.

Nedlukningsopgaven kræver stort overblik, en evne til at gøre det komplekse simpelt og modet til at prioritere. Gode kommunikationsevner er ligeledes vigtige for at få succes i jobbet. For være en succes i dette job vil struktur, analytiske evner og leder erfaring blive set som et plus.

Endelig er det en klar forudsætning, at du er fleksibel i forhold til, hvornår du afholder ferie, da nedlukningerne foregår i sommerferien og mellem jul og nytår. Vi forventer også at du behersker både dansk og engelsk i skrift og tale.

I Novo Nordisk stræber vi efter at være de bedste. Vi er førende i verden inden for diabetesbehandling og en større spiller indenfor behandling af blødninger, behandling med væksthormon og behandling med hormonterapi. Derfor kan vi tilbyde vores medarbejdere mulighed for en stærk professionel udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Jimmie Madsen på telefon + 45 3079 5992.

Ansøgningsfrist
27. april 2014.

Danmark - Bagsværd Produktion
10-Apr-2014 Rustfri Klejnsmed
Er du smed, har du hænderne skruet rigtigt på, og brænder du for at fremstille kvalitetsdele på et meget højt niveau, så har vi en spændende stilling til dig. Vi søger en klejnsmed til fremstilling af reservede...

Rustfri Klejnsmed

  • Produktion
  • Danmark - Bagsværd

Er du smed, har du hænderne skruet rigtigt på, og brænder du for at fremstille kvalitetsdele på et meget højt niveau, så har vi en spændende stilling til dig. Vi søger en klejnsmed til fremstilling af reservedele til produktionsmaskinerne hos Novo Nordisk på vores værksted i Bagsværd. Du kan se frem til et rigtig godt kollegialt sammenhold, til at sætte dit præg på arbejdspladsen og til at styrke dine kompetencer gennem sparring og uddannelse.

Om afdelingen
Finmekanisk Værksted fremstiller reservedele samt udvikler og modificerer dele til produktionsmaskinerne i Novo Nordisk. Vi fremstiller delene både som enkeltstyksproduktion og i mindre serier - primært i rustfast stål - og i henhold til de gældende krav inden for medicinalindustrien.

Jobbet
Du bliver en del af et team af dygtige kolleger, der er med til at holde produktionen i gang på Novo Nordisk’s fabrikker i Danmark og globalt. Dine opgaver bliver at udvikle og fremstille reservedele, prototyper og produktionsudstyr i rustfast stål til Novo Nordisk’s produktionsmaskiner. Du er med til at lave forbedringer og modificeringer af produktionsdelene og fremstiller selvstændigt dele i rustfast stål ud fra input fra dine kolleger i produktionen.

Opgaverne løses ofte i tæt samarbejde med maskinarbejdere fra værkstedet. Du kommer til at deltage i tværfaglige projekter, hvor du arbejder tæt sammen med specialister og håndværkere fra andre fagområder, og du vil komme til at rådgive dine kolleger om valg af udstyr og materialer. Du får også en del administrative opgaver i form af kontakt til vores underleverandører og opgavehåndtering.

Stillingen er kategoriseret i stillingskategori F3.

Kvalifikationer
Du er uddannet klejnsmed, og du har solid erfaring med både tyndpladebearbejdning og TIG-svejsning. Du kan bruge en kantpresse og er god til pladeudfoldning samt slibning og polering af rustfast stål. Du forstår standardiserede arbejdsprocedurer og tekniske tegninger og kan producere efter dem. Samtidig er du kvalitetsbevidst og kundeorienteret så opgaverne bliver løst tilfredsstillende og i høj standard.

Du trives på en arbejdsplads, hvor der bliver forventet noget af dig, og hvor alle er glade for at dele ud af deres viden og for at tage ansvar for det, de laver. Det er vigtigt, at du kan arbejde systematisk, overholde deadlines og bevare overblikket over flere opgaver. Dit PC kendskab er på brugerniveau, og du mestrer dansk og engelsk på 10. klasses niveau. Vi har en uformel tone og stor respekt for hinanden.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Uffe Bennov på +45 3075 8063 eller Sophus Monnerup på + 45 3075 4713.

Ansøgningsfrist
23. april 2014

Danmark - Bagsværd Produktion
09-Apr-2014 Supporter fyldeafdeling
I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her ha...

Supporter fyldeafdeling

  • Produktion
  • Danmark - Kalundborg

I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her handler ikke bare om at tjene til føden, men om at gøre en forskel. Finder du denne udfordring inspirerende og udfordrende er du er måske den nye supporter i vores tekniske support med ansvar for vores avancerede fyldelinier fra Bosch.

Om afdelingen
I Biopharm divisionen af Novo Nordisk har vi blandt andet ansvaret for at producere NovoSeven®, de kommende generationer af hæmofilipræparater, Glucagon og andre Biopharm produkter. Vi oplever en stigende efterspørgsel og har valgt at etablere en ny fabrik i Kalundborg for at sikre fyldning og pakning af vores produkter. Fyldefabrikken vil indeholde følgende processer; Vask og Sterilisation, Formulering, Fyld og Frysetørring.

Jobbet
Vores nye aseptiske fyldefabrik er udstyret med helt nye fyldelinier fra Bosch der netop nu er under kvalificering. Du skal primært supportere disse fyldelinier og det tilhørende perifere udstyr i det aseptiske område, med såvel daglige support som optimeringsopgaver. Du får mulighed for både at blive en vigtig GMP sparringspartner for drift teamets reparatører, der klarer de daglige praktiske vedligeholdelsesopgaver, og proceskemikere i deres arbejde med at sikre processer vedligeholdes og løbende optimeres.

Da du vil fungere som support for et team af kvalificerede reparatører, så vil det være en stor fordel du har have teknisk indsigt og forståelse for systemerne, så du på den ene side kan supportere og sparre med reparatørerne i dagligdagen ligesom du understøtte fabrikkens proces kemikere i deres arbejde med at sikre udstyrets validerede tilstand. Du vil få mulighed for selvstændigt at drive optimerings projekter i området, og i det hele taget være med til at sikre vores nye fyldelinier hver gang everer til tiden i verdensklasse.

Vi ser frem til at invitere dig ind i et team, der består af 21 fagligt dygtige, ambitiøse og målrettede medarbejdere og giver dig samtidig mulighed for at sætte dit præg på fremtidige arbejdsgange og de organisatoriske rammer.

Kvalifikationer
Du har formentlig en ingeniør eller maskinmester baggrund, og du har gennem din karriere opnået erfaring med drift, vedligehold og support opgaver af lignende systemer i den, gerne i den farmaceutiske industri.

Det forventes, at du anvender officepakken på et højt niveau, og du ubesværet kan tale og skrive engelsk.

Uanset din baggrund skal du have viden om GMP – gerne relateret til aseptisk produktion. Har du tilmed erfaring fra farmaceutisk produktion samt kendskab til kvalificering af udstyr, samt LEAN, er det absolut et plus.

Kvalitet og præcision er afgørende i vores industri, så det er vigtigt, at du er kvalitetsbevidst og har lyst til og har erfaring med skriftlig dokumentation der vil blive en stor del af dit arbejde Du formår proaktivt at etablere et godt arbejdsnetværk og gode relationer samt tænke optimering i enhver arbejdsopgave. Sidst, men ikke mindst, er du er udadvendt og god til at kommunikere på tværs af faggrænser – både på dansk og engelsk.

I Novo Nordisk stræber vi efter at være de bedste. Vi er førende i verden indenfor diabetesbehandling og en større spiller indenfor behandling af blødninger, behandling med væksthormon og behandling med hormonterapi. Derfor kan vi tilbyde vores medarbejdere mulighed for en stærk professionel udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Peter René Jensen på +45 3079 2663.

Deadline
25.april 2014