Qualified Person - QP (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, Shigella and Zika.

We are currently looking for a motivated Qualified Person - QP (m/f/d) to join our Quality Assurance Department in Vienna. Your Key responsibilities will involve working with vaccine products, overseeing technology transfers, and ensuring strict adherence to Good Manufacturing Practices. In detail you will be working on tasks such as:

• Act as a Qualified Person (QP) for two of our products IXIARO and IXCHIQ, ensuring compliance with EU GMP regulations (Annex 16) for Batch Certification across all markets, including all associated QP responsibilities
• Prepare documents which require QP-approval as per EU or local requirements
• Collaborate with Commercial Operations and Supply Chain Management on all quality-related matters to support operational needs
• Participate in local and global Quality Harmonization/Consolidation Projects regarding Product Certification and other QP-related topics
• Participate in supplier audits and regulatory inspections
• Actively support further development of the Quality Assurance Department by providing professional experience related to the performance of Quality Systems
• Actively support Quality Assurance activities related to authority and 3rd party inspections
• Update job knowledge with all regulatory requirements and development in quality management, participating in educational opportunities relating to the work of Valneva

Requirements

• University degree in life sciences with substantial GMP experience in the Pharma or Biotech industry
• At least 3-4 years of experience in a GMP-regulated environment
• Certified by a Competent Authority to act as a Qualified Person (QP) per EU legal requirements (compulsory) as well as 1-2 years of experience as QP
• Proficient in technology transfer processes and GMP manufacturing operations
• Proven experience in working with commercial products
• Leadership capabilities as a plus and strong project management skills
• Strong analytical skills, able to structure and interpret complex information effectively
• Skilled in drafting clear, well-argued documents
• Excellent communication skills and social competence, with a proactive, team-oriented mindset
• Customer-focused approach and adept in conflict management
• Fluency in both written and spoken English

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
• Lifelong learning: Unlimited access to LinkedIn Learning & German/English courses for free
• Health & Wellbeing: Free access to sports and fitness activities via myClubs

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 € 90.000 gross per year based on full-time employment. However our salaries are market oriented and in line with your qualifications and experience.