QC Scientist for Stability

Are you ready to be part of an innovative, international vaccine company committed to making a real difference by protecting lives every day? Do you thrive in a collaborative environment alongside a team of passionate QC Scientists and Technicians?

If so, then we have an exciting opportunity for you!

Are you our next pioneer?

At our fast-growing company, we´re dedicated to protecting lives every day through the development and production of essential vaccines. As a QC Scientist for Stability, you´ll play a crucial role in ensuring the quality and efficacy of our products. The role is placed at our manufacturing site in Kvistgaard and you will report to the Director of QC.

In the QC Scientist role, you will be able to shape our processes. Your responsibilities will include:

  • Defining test programs for vaccines
  • Implementing new stability studies and analysis
  • Preparing stability protocols, establishing stability studies, and reporting data and trends
  • Maintaining ongoing stability studies
  • Ensuring all activities adhere to cGMP standards
  • Writing deviations, CAPAs, change controls, handling external OOS/OOT, and quality SOPs
  • A Coordinating role for stability studies for the various projects within the QC team (Point of contact)

About the QC Department

We are a team of +60 skilled and dedicated employees in QC in Denmark divided into seven teams: QC Stability, QC Biochemistry, QC Microbiology, QC Raw Materials, QC Sample Manager, QC Externals, and QC Sample Flow. The QC department in Kvistgaard is working under cGMP in close collaboration with our QC department in Munich.

The Stability team prepares a broad variety of stability studies to support production and shelf life for clinical studies, and commercial vaccines. The team is responsible for ensuring stability protocols, execution, and reporting of stability data for all our vaccines in both bulk drug substance and filling production and at CMOs.

QC Stability works in close collaboration with a broad range of departments, such as Process Development, external laboratories, and Quality Assurance.

We offer an informal working environment, with a flexible attitude, working as one team where we support each other to reach our deadlines.

Who are you?

To succeed in this role, you´ll need:

  • A Master´s or Ph.D. degree eg. biochemist, chemist, pharmacist, biologist, or as like
  • 3-5 years of experience in the pharmaceutical industry from an Analytical Development, Quality Assurance, or Quality Control department
  • Experience working in a GMP environment, preferably with stability
  • Strong coordination skills and the ability to work across departments
  • A quality-minded and structured mindset

You possess strong analytical and pragmatic abilities, effortlessly managing multiple tasks while maintaining a comprehensive perspective. Project work comes naturally to you, as you embrace change, demonstrate flexibility, and exhibit excellent cooperation skills. You enjoy sharing your expertise and engaging in open, professional communication. A good sense of humor would complement your qualities, making you an ideal fit for the team.

Does this appeal to you?

We are interviewing on an ongoing basis and look forward to receiving your CV as soon as possible.

For us, it is all about improving and saving lives

We are a fully integrated vaccine company focused on the development, manufacturing, and commercialization of vaccines, and our vision is to become one of the largest pure-play vaccine companies in the world. At Bavarian Nordic, you will be part of a global team of +1600 dedicated colleagues worldwide, all passionate about making a difference. We offer an inclusive and flexible workplace with a strong focus on personal and professional development, and we welcome people who share our passion for saving lives. If you are open-minded and have the willpower to succeed, we might be a perfect fit for you.

Our employees also have the advantage of being able to use our bus route, 70E, which runs from Humlebæk Station directly to our production facilities in Kvistgaard. The bus has four departures every morning and afternoon with scheduled stops at Hørsholmvej and Kvistgaard St.

The new service improves the commuting experience to and from Kvistgaard, where some of our employees can now benefit from a significant time savings of almost 40 minutes each way, making their daily commute more efficient and convenient.




Founded in 1994, we have more than 25 years of experience in developing life-saving vaccines. We are a global leader in smallpox and mpox vaccines. Our commercial product portfolio contains market-leading vaccines against rabies and tick-borne encephalitis and an Ebola vaccine. We are a global company headquartered in Denmark with a state-of-the-art production facility and sites in Germany, Switzerland, and USA. Our values – our Bavarian Nordic DNA, as we like to call it – are what guide our actions every day. We act as persistent pioneers, embrace change, value being boosted by the team, and believe in protecting lives every day. If that is also a part of your DNA, we invite you to join us in Bavarian Nordic! Bavarian Nordic is an Equal Opportunity Employer.
www.bavarian-nordic.com

Join Bavarian Nordic a fully integrated vaccine company focused on the development, manufacturing and commercialization of life-savings vaccines.

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Iben Schildt Sørensen 
Director, QC
+45 21 34 98 88