QA Professional
- Quality
- Denmark - Gentofte
Would you like to join us in making a difference to people in need of glucagon and growth hormone. Would you like to be responsible for quality assurance of qualification and validation tasks? A job is waiting for you in a challenging and developing environment.
About the department
In Biopharm QA API Gentofte you will join a team with 6 engaged employees. Together we assure quality and compliance in the production of growth hormone and glucagon. The working relations are informal and the team values professional sparring and good humour highly. The team responsibility covers the release of the product, approval of instructions and qualification and validation, processing of change and nonconformity cases and various other tasks.
The job
You are responsible for qualification and validation of the challenging and changing facilities for manufacture of hGH and glucagon. The facilities face major changes and challenging tasks within IQ, OQ, PQ computer and cleaning validation. An important element of the job involves cooperation with the project team, production department and process QA. Quality is the key words and therefore it is natural for you to have an ongoing dialogue and good relations with your stakeholders regarding how we ensure quality and compliance. 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. When you start you will undergo an individual and intense training program.
Qualifications
You have a Master of Science degree. You are familiar with GMP and the requirements of the authorities in the pharmaceutical industry. Ideally you have several years of experience within validation and qualification. You work systematically and can take a comprehensive view and you are not afraid of taking decisions. Moreover, you are purposeful and able to prioritise several tasks in a changing environment
Precise communication is absolutely essential and you must be capable of taking part in constructive cooperation concerning the various tasks and have the kind of impact that means you can stand firm in favour of product and user safety. Your language skills cover proficiency in both Danish and English.
Feel free to submit your job application in either English or Danish, whichever you prefer.
At Novo Nordisk we use our skills, dedication and ambition to help people in need of glucagon and growth hormone. By working with us you will have the opportunity to do the same in a global business environment.
Contact
For further information, please call Lotte Solvang Christensen on +45 3075 8846 or Ulla Falkenberg on +45 3075 8890.
Learn more about Novo Nordisk ProductSupply and working in QA using this link www.novonordisk.com/careers/QA.
Deadline
29 September 2013.
- Quality
- Denmark - Gentofte
Would you like to join us in making a difference to people in need of glucagon and growth hormone. Would you like to be responsible for quality assurance of qualification and validation tasks? A job is waiting for you in a challenging and developing environment.
About the department
In Biopharm QA API Gentofte you will join a team with 6 engaged employees. Together we assure quality and compliance in the production of growth hormone and glucagon. The working relations are informal and the team values professional sparring and good humour highly. The team responsibility covers the release of the product, approval of instructions and qualification and validation, processing of change and nonconformity cases and various other tasks.
The job
You are responsible for qualification and validation of the challenging and changing facilities for manufacture of hGH and glucagon. The facilities face major changes and challenging tasks within IQ, OQ, PQ computer and cleaning validation. An important element of the job involves cooperation with the project team, production department and process QA. Quality is the key words and therefore it is natural for you to have an ongoing dialogue and good relations with your stakeholders regarding how we ensure quality and compliance. 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. When you start you will undergo an individual and intense training program.
Qualifications
You have a Master of Science degree. You are familiar with GMP and the requirements of the authorities in the pharmaceutical industry. Ideally you have several years of experience within validation and qualification. You work systematically and can take a comprehensive view and you are not afraid of taking decisions. Moreover, you are purposeful and able to prioritise several tasks in a changing environment
Precise communication is absolutely essential and you must be capable of taking part in constructive cooperation concerning the various tasks and have the kind of impact that means you can stand firm in favour of product and user safety. Your language skills cover proficiency in both Danish and English.
Feel free to submit your job application in either English or Danish, whichever you prefer.
At Novo Nordisk we use our skills, dedication and ambition to help people in need of glucagon and growth hormone. By working with us you will have the opportunity to do the same in a global business environment.
Contact
For further information, please call Lotte Solvang Christensen on +45 3075 8846 or Ulla Falkenberg on +45 3075 8890.
Learn more about Novo Nordisk ProductSupply and working in QA using this link www.novonordisk.com/careers/QA.
Deadline
29 September 2013.