QA Professional
- Quality
- Denmark - Hillerød
Would you like to join us in making a difference to people with haemophilia? 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 Hillerød you will join a team with 11 engaged employees. Together we assure quality and compliance in the production of new haemophilia API. The working relations are informal and the team value 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 non-conformity cases and various other tasks.
The job
You are responsible for qualification and validation of a challenging and changing facility for manufacture of new haemophilia products. The facility is on-going major changes and is facing 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 on-going dialogue and good relations with your stakeholders regarding how we ensure quality and compliance.
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 with Haemophilia, and change their lives. By working with us you will have the opportunity to do the same in a global business environment.
Learn more about Novo Nordisk ProductSupply and working in QA using this link
www.novonordisk.com/careers/QA
Contact
For further information, please call Lars Nyholm on +45 3075 5226 or Hans Koch on +45 3079 9825.
Deadline
18. August 2013
- Quality
- Denmark - Hillerød
Would you like to join us in making a difference to people with haemophilia? 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 Hillerød you will join a team with 11 engaged employees. Together we assure quality and compliance in the production of new haemophilia API. The working relations are informal and the team value 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 non-conformity cases and various other tasks.
The job
You are responsible for qualification and validation of a challenging and changing facility for manufacture of new haemophilia products. The facility is on-going major changes and is facing 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 on-going dialogue and good relations with your stakeholders regarding how we ensure quality and compliance.
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 with Haemophilia, and change their lives. By working with us you will have the opportunity to do the same in a global business environment.
Learn more about Novo Nordisk ProductSupply and working in QA using this link
www.novonordisk.com/careers/QA
Contact
For further information, please call Lars Nyholm on +45 3075 5226 or Hans Koch on +45 3079 9825.
Deadline
18. August 2013