Senior CMO Manager (m/f/d)
We are a specialty vaccine company that develops, manufactures, and commercializes prophylactic vaccines for infectious diseases addressing unmet medical needs.
We have leveraged our expertise and capabilities both to commercialize three vaccines, including the world's first and only chikungunya vaccine, and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease and Zika.
With operations in Austria, Canada, France, Sweden, the United Kingdom, and the U.S., we are committed to making a positive impact on global public health.
Together, we are a global Company which is open to people of all backgrounds. Our diverse and inclusive workforce makes Valneva a great place to work.
Our CMO Management Team are now recruiting for a Senior CMO Manager.
Your Responsibilities
- Serve as the technical contact for external manufacturing partners (Fill & Finish, Visual Inspection and Packaging) and internal production teams.
- Support commercial manufacturing by reviewing process changes, deviations, CAPAs, and Change Controls.
- Contribute to technical projects, including process improvements, capacity optimization, technology transfers, and product launches.
- Perform technical assessments and support risk management activities across the product lifecycle.
- Collaborate with Quality and Regulatory Affairs to review technical documentation, including Master Batch Records, risk assessments, and qualification protocols.
- Participate in troubleshooting activities and identify opportunities for continuous process improvement.
- Foster effective communication and collaboration with internal stakeholders and external manufacturing partners.
What You Bring
- Master's degree in Life Sciences, Biotechnology, Pharmacy, Chemical Engineering, or a related scientific discipline.
- 2–3 years of experience in a cGMP-regulated pharmaceutical or biotechnology manufacturing environment, ideally within Technical Operations, MS&T, or commercial manufacturing.
- Sound understanding of pharmaceutical manufacturing processes and GMP requirements.
- Experience working with external manufacturing partners or in a cross-functional, matrix organization.
- Knowledge of Change Control, post-approval changes, ICH guidelines, regulatory validation, and quality systems is an advantage.
- A proactive, hands-on approach with strong project management, problem-solving, and organizational skills.
- Excellent communication and stakeholder management skills, with the ability to build effective working relationships across functions and sites.
- Fluent in English; German is considered an advantage.
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
Join us and shape the future of biotechnology!
Due to legal reasons we are obliged to disclose the minimum salary for this position, which is € 60.000 gross per year based on full-time employment. However our salaries are market oriented and in line with your qualifications and experience.
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