Job at a glance
Can you investigate a deviation and get to the real root cause? Do you get satisfaction from improving a process without compromising quality? And would you rather help build and improve something than simply maintain it? Then you may be the person we are looking for at Bavarian Nordic in Kvistgaard. You will drive deviation investigations, strengthen our SOP landscape, support audit and inspection readiness, and identify and implement improvements that make our daily operations more robust and efficient.
You will report directly to the Head of Site Supply Chain and work closely with our Warehouse Manager, warehouse operators, QA and colleagues across the site. As this is a newly created position, you will have a real opportunity to shape the role and contribute to the continued development of our warehouse operations. What you will do Drive deviation investigations and CAPAs You will drive deviations related to warehouse and supply chain processes from identification and classification through structured root cause investigation and impact assessment to CAPA definition and follow-up.
You will ensure investigations progress to closure and that conclusions and actions are technically sound, well documented and inspection-ready. You will work closely with Warehouse, QA and relevant stakeholders to ensure that corrective and preventive actions address the actual root cause and deliver sustainable improvements. Own and strengthen our SOP landscape You will take an active ownership role in the SOP landscape for warehouse and relevant supply chain processes.
This includes writing new procedures, revising existing ones, coordinating periodic reviews and ensuring that our procedures reflect both regulatory requirements and the way we operate. You will also help ensure that training curricula and relevant system reviews remain current and effective. Drive process optimization Compliance and efficiency should reinforce each other. You will identify gaps, risks and bottlenecks, and turn them into practical improvement initiatives without compromising the quality requirements under which we operate.
You will drive improvements from initial idea and root cause through implementation and embedding into daily operations. Audit and inspection readiness You will support preparation for internal audits and regulatory inspections and participate as a key Supply Chain representative for warehouse-related compliance topics. You will coordinate follow-up activities and help ensure that we remain inspection-ready — not only when an inspection is approaching, but as part of our everyday way of working.
You will act as the bridge between regulatory requirements and daily operations. You can translate complex GMP and GDP requirements into practical solutions that warehouse operators, managers, QA and other business stakeholders can understand and work with. You will collaborate across functions and levels of the organization and contribute to building a strong quality and continuous-improvement culture within Site Supply Chain.
What we are looking for A degree in Pharmacy, Engineering, Biochemistry, Microbiology, or another relevant scientific discipline Experience from a regulated environment such as pharmaceuticals, biotechnology, medical devices, food production, or a similar industry Hands-on experience owning deviations, change controls and CAPAs independently Experience participating in internal audits and regulatory inspections Experience with LEAN or continuous improvement.
Yellow or Green Belt is an advantage Working knowledge of ERP systems (D365 F&O or similar) Fluent in Danish and English, written and spoken, with strong technical writing skills Experience with Power BI is an advantage A proactive and structured mindset, combined with the ability to follow initiatives through to completion Confidence working independently and making decisions within established procedures and quality requirements Experience from warehouse, logistics, s