QA Professional with flair for analytical chemistry
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Gentofte
- Quality
- Gentofte
Biopharm QA is looking for a talented and ambitious QA Professional with flair for analytical chemistry. You will be a part of a team with the quality assurance responsibility for the Quality Control laboratories primarily in Gentofte and occasionally in Hillerød and Kalundborg.
About the department
The department “Biopharm QA QC & MDev” consists of two teams, one team responsible for quality assurance of QC laboratories and one team responsible for quality assurance of manufacturing development (MDev) including product stability and specifications. Our key task is to review and approve GMP documentation in order to ensure delivery of high-quality products in compliance with regulatory requirements. We know that simplicity and quality go hand in hand and accordingly we embrace changes and are brave to make our quality decisions based on increased simplicity and digital solutions.
As QA Professional in Biopharm QA QC & MDev you will join a group of 20 highly skilled and competent colleagues. By joining us you will get the chance to obtain professional and personal development and you will get an excellent and unique overview of current authority expectations and demands in the pharmaceutical industry. You will become part of a team which has a high level of self-governance. The working relations are informal and the team values professional sparring and good humour.
The job
The job is mainly situated in Gentofte and the team consists of 7 QA Professionals. The job includes QA review of several types of documents such as validation reports, change requests and deviations. The analyses performed are for example HPLC, Spectroscopy, Bio and Immunoassay and general pharmacopeia methods including microbiology.
Your main responsibility will be to assure the QC laboratories deliver high quality test results and that these are performed in full compliance with the legislation. QA is regularly present in the QC laboratories to have a good understanding on how the tests are performed and to provide guidance on quality matters.
Qualifications
You hold a master’s degree within pharmacy, chemistry, microbiology or similar.
You are flexible and have a strong quality mind-set combined with the ability to simplify processes. You meet your deadlines, and you know how to prioritise between different tasks in a dynamic environment. You like and are good at coordinating different tasks for both yourself and other people and you demonstrate an ability to find the right solutions with your colleagues in your own team and across areas. 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, compliance and business needs. At the same time, you perform well in a team-oriented environment where you seek collaboration and acknowledge your colleagues.
The position is temporarily for 24 months.
Your application should be in English.
Contact
If you want to know more about the position, please contact Tanja Thorskov Bladt +453075 5155.
Deadline
10 November 2019.
Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
Information og data
Denne ledige stilling har jobtypen "Laborant", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Gentofte.
Jobbet er oprettet på vores service den 24.10.2019, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Laborant
- Gentofte
- Søndag den 10. november 2019
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