Quality Assurance of biopharmaceutical products and processes

Novo Nordisk A/S





Gentofte, Capital Region of Denmark, DK

Biopharm Quality Assurance (QA) is looking for a talented and ambitious QA Professional. You will be part of a team with the quality assurance responsibility for the area Manufacturing Development.

About the department
The department “Biopharm QA QC & MDev” consists of two teams, one team responsible for quality assurance of Quality Control (QC) laboratories and one team responsible for quality assurance of Manufacturing Development (MDev) including product stability and specifications. Our key task in QA is to review and approve GMP documentation in order to ensure delivery of high-quality products in compliance with regulatory requirements.

As QA Professional in Biopharm QA QC & MDev you will join a group of 15 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 overview of current authority expectations and demands in the pharmaceutical industry. In addition, you will learn about our unique products within haemophilia and growth disorders. Products that everyday help patients live a better life. 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 situated in Gentofte and the team consists of 6 QA Professionals. After a thorough introduction to our products and processes you will be responsible for quality assurance regarding development documentation, specifications, stability studies, change requests and deviations in the area Manufacturing Development.

QA is regularly present in the laboratory and pilot facilities in Manufacturing Development to have a good process understanding and to provide guidance on quality matters.

You hold a master’s degree within pharmacy, engineering or similar and is one of the best from your year group. You have a good understanding of the process for manufacturing of biopharmaceutical drugs.

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. Your language skills cover proficiency in both Danish and English.

You work independently 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 for 24 Months.

Your application must be in English.

If you want to know more about the position, please contact Erik Steffensen at 3079 3019.

08 March 2020.

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.

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Ansøgningsfrist d. 08.03.2020
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Novo Nordisk A/S - hurtigt overblik

Novo Nordisk A/S
Novo Nordisk A/S
Novo Nordisk is a global healthcare company with more than 90 years of innovation and leadership in diabetes care. This heritage has given us experience and capabilities that also enable us to help people defeat other serious chronic conditions: haemophilia, growth disorders and obesity.

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