QA Specialist for QC

Are you ready to make a difference in global health by ensuring the highest quality standards in vaccine production, contributing to the mission of saving lives?

We are looking for our new QA Specialist supporting QC. A broad role covering many different aspects. If this sounds interesting to you, then continue reading!

About the team

The QA Operations organization consists of 45 employees, 5 managers, and one director. You will be part of the dynamic QA for QC, Raw Materials, and Warehouse team which consists of 6 employees in Germany (2) and Denmark (4). The team supports QC with processing of deviations, change controls, laboratory investigations, stability, validation and qualification of analytical methods and equipment as well as the release of Raw Materials and Secondary Packaging Materials for use in Production.

You will report to the Manager for QA for QC, Raw Materials and Warehouse. The position is based in Denmark and requires you to be mainly on-site in Kvistgaard.

“As a leader, I believe in an open-door policy where accessibility and transparency are at the core of my approach. I'm deeply committed to supporting my team's success by prioritizing their professional growth and mental well-being. My goal is to create a balanced, thriving work environment where every employee feels valued and empowered.” - Says Anabelle Legarth Honoré, Manager for QA for QC, Raw Materials and Warehouse.

Your impact

This position primarily focuses on ensuring QA support to QC, including:

• Review and approve SOPs, Change Control, Deviations and CAPAs in Veeva
• Handling of Out-of-Specification (OOS) and Laboratory Investigations
• Review and approval of protocols and reports for Analytical Method Validation and Equipment Qualification as well as supporting related projects
• Review and approval of Stability protocols and reports
• Continuous Improvement activities

Are you our next pioneer?

Succeeding with our vision of becoming one of the largest pure-play vaccine companies in the world is no walk in the park, and that is why we need people like you who are determined to make it happen and have the following qualifications:

• A relevant MSc degree (Pharmacology, Biochemistry, Microbiology, Life Sciences, or similar)
• A minimum of 5 years of experience from a similar position as QA
• Solid GMP knowledge
• Experience with Quality Risk Management and Systematic Problem Solving
• Fluency in English, both written and verbal

About you

You have excellent stakeholder management and collaboration skills, strong communication, and a proactive, open-minded approach. You are decisive, and optimistic in problem-solving, with a drive to achieve goals and manage changing priorities in fast-paced settings. Adaptable, flexible, and resilient, you thrive in dynamic environments, balancing quality with pragmatic solutions. You are accountable, detail-oriented, and confident working both independently and in teams, especially in international contexts.

Why join us?

• We offer great collegiality, and daily team meets to ensure alignment and support to team members
• As we continue to grow, you will have a unique opportunity to make a real impact, shaping both the team and our QA processes
• Opportunity to take part in exciting projects supporting QC, including the insourcing of QC release testing, with the chance to be a key driver in analytical method validation initiatives
• We provide an international environment where personal and professional growth is highly prioritized
• Become part of a team that directly contributes to global health by manufacturing and developing life-saving vaccines
• Enjoy a vibrant staff club that offers a variety of diverse and exciting events
• We have charging stations for electric vehicles at our facilities in Kvistgaard
• Convenient bus route (70E) from Humlebæk Station directly to our Kvistgaard facilities

Ready to make a difference? Apply now!

Apply by clicking the ‘APPLY’ button. We are interviewing on an ongoing basis and look forward to receiving your motivated CV as soon as possible. It is not mandatory to send a cover letter. Applications submitted via email will not be considered.

Please contact Anabelle Legarth Honoré, QA for QC Manager Raw Materials, and Warehouse at +45 20 22 73 08, if you have any questions about the role.

Join us and become part of a diverse team dedicated to making a difference together.

For us, it is all about improving and saving lives

Improving and saving lives through innovative vaccines is at the heart of what we do in Bavarian Nordic. We are a