Senior Manager Lab Coordination
Confirmed on the employer's own hiring board on Oct 31, 2026. First seen by Alion on Oct 27, 2026.
At Valneva, we are dedicated to developing innovative vaccines that protect people worldwide against serious infectious diseases.
We are looking for a Senior Manager Lab Coordination (m/f/d) to join our Quality Control team. In this role, you will be responsible for the planning, coordination and execution of lab coordination activities supporting the GMP laboratory. Additionally to your own operational tasks you will lead and develop a small lab coordination team (3 people) with the support of the Head of Quality Control. You will work closely with internal departments, clients, and external testing laboratories.
Responsibilities
- Coordination of day-to-day Lab activities, working hands-on alongside the team
- Person in charge/support for operational readiness and GMP compliance of laboratory equipment, computerized systems and laboratory infrastructure
- Person in charge/support for qualification, validation, maintenance and lifecycle activities for analytical and storage equipment and relevant QC systems
- Validation Officer for equipment and computerized systems and management of related quality events and documentation
- Person in charge/support for qualification, availability and inventory management of key reagents, reference substances, controls, chemicals and laboratory consumables
- Coordination of daily activities and priorities of the Lab Coordination team (3 employees)
- Collaboration on operational and technical CAPEX planning
Requirements
- Academic degree in Life Science or another relevant scientific field, with at least 5 years of experience in the life science or pharmaceutical industry in a GxP-regulated environment (ideally involving vaccines)
- Experience with QC Lab operations in GxP regulated life science or pharmaceutical industry subject to FDA and other global regulatory authority inspections is preferred
- Experience with Equipment / Analytical Instruments Qualifications is preferred
- Good knowledge of relevant GxP legislation for EU, US and other global highly-regulated markets
- Good organizational, documentation management and teamwork skills
- Open-minded and innovative / creative team-player
- Fluent in English, fluent in German is preferred
Benefits
Working with Valneva means being part of a global biotech company with a clear vision to make a meaningful impact in the world. At Valneva, you can expect a dynamic and innovative work environment characterized by an open, appreciative company culture and exciting, impactful assignments. Enjoy the benefits of flat hierarchies, an international atmosphere, and regular company events that foster collaboration and connection.
Additionally, we offer:
- Work Life Balance: Flexitime & Compensation days
- Financial perks: Performance-related bonus & Lunch vouchers
- Health & Wellbeing: Free access to sports and fitness activities via myClubs & Office Massages
Minimum Annual Salary: EUR 60,000 gross per year. The actual salary offered will be determined based on the candidate’s qualifications, professional experience, and skills, with a willingness to overpay the applicable minimum salary.
Join us and shape the future of biotechnology!