Senior QA Specialist

Are you passionate about ensuring compliance in a regulated environment and upholding the highest standards in pharmaceutical regulations? Do you aspire to be part of a multinational company where you can work within a global team dedicated to patient safety and product quality?

Great! We have an exciting opportunity for you as we are seeking a highly skilled QA Senior Specialist to join our Corporate Audit and Inspection team.

Boost our Team
As a key member of our dedicated team of 8 passionate QA professionals, you will play a crucial role in our mission. You will be part of a global, fully integrated vaccine company committed to saving lives and improving health worldwide through groundbreaking vaccines.

• We are a small, yet expanding global team
• Our mission is to ensure full compliance with GMP regulations across all Bavarian Nordic suppliers
• We oversee the implementation of GMP standards across all internal departments and processes
• In this role, you will work in a hybrid capacity based in Kvistgaard, Denmark, reporting directly to the Associate Director of Audits & Inspections, located in Switzerland

Your Impact
Our vaccines make a real difference to people, and no matter your role we all contribute to protecting lives every day. Your tasks will be:

• Global Quality Agreement Management
• Global Inspection Management
• Conducting Internal Audits in the cGMP area
• Help developing processes in the Audit & Inspection department
• Be a respondent for GMP topics, Quality Agreements, Internal Supplier requests

Are you our next pioneer?
Succeeding being 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. Your qualifications:

• Degree in Natural Sciences (BSc., MSc., PhD)
• Minimum of 5 years experience in a GxP environment
• Strong expertise in managing Quality Agreements particularly within the Supplier Qualification process
• Deep knowledge of quality standards, including GMP and ISO
• Profound knowledge of QA processes
• Ideally you have expertise in the management of Internal Audits and management of regulatory updates
• Fluent in English

About you

• You are a proactive, change-driven individual who thrives on adapting to new challenges
• You excel in responding effectively to evolving work demands
• Your strong communication and collaboration skills are complemented by a high level of diplomacy
• You are well-versed in navigating international GMP regulations and collaborating with global suppliers

Why join us?

• Make a Global Impact: Be part of a team that directly contributes to global health by manufacturing and developing life-saving vaccines. Your work here has a visible and significant impact, ensuring the safety and well-being of millions
• Dynamic Vaccine Industry: Join the fascinating field of vaccine production, where every day brings new challenges and opportunities to protect public health
• Global Collaboration: Work within a global department, managing inspections and ensuring the highest standards are met across our worldwide operations
• Engaging Workplace Culture: Enjoy a vibrant staff club that offers a variety of diverse and exciting events, fostering a strong sense of community and work-life balance

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 fully integrated vaccine company focused on the development, manufacturing, and commercialization of life-saving vaccines, and we are one of the largest pure-play vaccine companies in the world.

In Bavarian Nordic, we believe in the power of the team, and you will be part of a global team of more than +1600 dedicated employees with diverse backgrounds and viewpoints, who are bound together by our commitment to protect lives every day. We believe in creating an inclusive and flexible workplace with a strong focus on personal and professional development, because we need each other to take things further.

We operate in a world in constant flux and always explore new opportunities. So, if you are open-minded and have the willpower to succeed, we might be a perfect fit for you.

Ready to make a Difference? Apply Now!
We are interviewing on an ongoing basis and look forward to receiving your CV and Motivating Application as soon as possible. Applications sent by email will not be considered.

For questions about the role, please contact Torsten Wehren, Associate Director Audits & Inspections at +41(31) 8885121.

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

Location: Kvistgaard - Hejreskovvej 18