QC & LIMS Release Lead — Drive Quality & IT Collaboration

Bavarian Nordic A/S; Denmark; On-site; DKK 1,000,000 - 1,400,000; Full time

Job summary

Bavarian Nordic A/S is seeking a QC Manager for LIMS & Release to lead a 12-person sub-team within QC and to align release activities with manufacturing and QC needs. You will drive daily operations, ensure data integrity and guide staff development while maintaining cGMP compliance and robust LIMS support across LabVantage.

You will collaborate with IT, manufacturing and end-users to optimize workflows and deliver reliable system performance in a fast-paced vaccine manufacturing environment.

Qualifications

• Relevant scientific degree in GMP pharma/biotech environments.
• Experience with LIMS and controlled methods, specs and data.
• Understanding of raw material release and CoAs processes.
• Solid GMP, data integrity and Quality Management exposure.
• Leadership experience with people development.

Responsibilities

• Lead a team with diverse release, support and LIMS duties.
• Create shared direction across release activities and daily work.
• Provide coaching and development plans for staff.
• Ensure dependable daily delivery and performance.
• Oversee workload, priorities and risks across releases and CoAs.
• Balance daily tasks with LabVantage project needs.
• Maintain compliant systems and processes.
• Ensure CGMP compliance and QA alignment.
• Promote data integrity and accurate documentation.
• Coordinate with QC end-users, IT and manufacturing.
• Use data to improve workflows and transparency.

Skills

People leadership

Prioritisation & planning

Cross-functional collaboration

Communication

Change management

Education

Scientific degree (GMP pharma/biotech)

Tools

LabVantage

LIMS

Job description

Bavarian Nordic A/S is seeking a QC Manager for LIMS & Release to lead a 12-person sub-team within QC and to align release activities with manufacturing and QC needs. You will drive daily operations, ensure data integrity and guide staff development while maintaining cGMP compliance and robust LIMS support across LabVantage.

You will collaborate with IT, manufacturing and end-users to optimize workflows and deliver reliable system performance in a fast-paced vaccine manufacturing environment.