QA Professional for assembly and packaging production lines

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Måløv

  • Quality
  • Måløv

Are you ready for a position in a department who is responsible for releasing finished products to patients worldwide? Our department in Biopharm QA is responsible for assuring the quality of every step of the production, which covers production, assembly and packaging at three different sites: Måløv, Værløse and Gentofte.

Your primary location will be in Måløv, but due to our unit´s location at different sites, some flexibility will be expected in connection with seminars, workshops, meetings and collaboration in general.

About the department

We are a dynamic department with 20 employees divided into two teams and are responsible for the quality assurance of our pharmaceutical products ranging from tablets to finished packed products. You will become part of a dedicated team of academics who are focused on ensuring GMP in a packaging department in Måløv.

The Job

As a Quality Assurance (QA) professional you are the gatekeeper for GMP compliance. After a period of introduction and training it will be one of your primary responsibilities to ensure review of batch documentation including approval/rejection of assembly and packaging orders according to GMP and our Standard Operating Procedures (SOP).

You are able to coordinate several tasks with different deadlines and thrive in a dynamic and flexible team. To succeed in this job, it is important to have a close and good collaboration with our production and being able to communicate with a wide range of people. Furthermore, performing QA oversight by being present in our production facilities.

As part of the QA team you will have the opportunity to work with highly skilled people and get a solid understanding of GMP and manufacturing processes in a packaging department. The work environment is informal, and the team is characterised by a high quality mind-set and a cooperative spirit.

Qualifications

You have a master’s degree in pharmacy, engineering or similar and preferably some GMP experience from the pharmaceutical industry. It will be an advantage if you have some level of IT flair and knowledge of digitalisation tools, as we are facing a lot of new exciting opportunities to improve our processes through digitalisation.

You communicate clearly and have a structured approach to ensure that complex problems appear logically and coherently, in Danish and as well in English.

Working at Novo Nordisk

At Novo Nordisk your skills, dedication and ambition help us change lives for the better. In return we offer you a chance to work with highly skilled people and benefit from a wide range of possibilities for personal and professional development.

Contact

For further information, please contact Christina Halberg at +45 3075 9031.

Deadline

28 June 2020. Applications are reviewed on a rolling basis, so please apply as soon as possible.

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 "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".

Arbejdsstedet er beliggende i Måløv.

Jobbet er oprettet på vores service den 9.6.2020, 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.
  • Forretningsudvikler
  • Måløv
  • Søndag den 28. juni 2020

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