Head of Quality Control (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.

Responsibilities

We are currently looking for an experienced and proactive Head of Quality Control (m/f/d) on-site in Vienna. Reporting directly to the Site Director of Quality, you will be contributing to strategic decisions while leading the QC team in a dynamic and purpose-driven environment. Your role will be pivotal in ensuring that all testing processes align with stringent internal quality standards and external regulatory requirements, including compliance with §70 AMG and §9 AMBO 2009. Your Key Responsibilities will include:

• Lead and develop the local QC team, including QC Center of Expertise, QC Lab Operations, and Lab Support teams
• Oversee QC testing for release, stability, and raw materials, as well as sample management for QC and Development labs
• Maintain facilities and equipment to ensure functionality and suitability for QC purposes
• Collaborate with stakeholders in Supply Chain and Development to align QC testing with project timelines
• Ensure compliant operations of the in-vivo QC testing in collaboration with the Laboratory Animal Facility
• Manage analytical method transfers and external QC testing activities effectively
• Stay updated on cGMP guidelines, pharmacopeia requirements, and scientific advancements in QC testing methods
• Ensure compliance with all internal and external Environment, Health, and Safety regulations for QC staff, facilities, and processes
• Define and manage the QC budget (CAPEX and OPEX) to ensure efficient operations and timely delivery of QC results
• Proactively escalate significant quality issues related to QC operations to ensure resolution and transparency

Requirements

• Master’s degree (or higher) in Life Sciences with a minimum of 5 years of relevant industry experience
• Extensive management experience within Quality Control, Lab operations in GxP regulated life science or pharmaceutical industry
• Proven experience hosting inspections by FDA and other global regulatory authorities
• Deep knowledge of GxP regulations (GMP, GDP, GCP, GCLP) for EU, US, and other highly regulated markets
• Strong management and leadership abilities to inspire and engage multicultural, diverse teams
• Excellent interpersonal communication and assertiveness skills, with the ability to influence and collaborate across functions
• A proactive, innovative, and solution-oriented mindset, able to thrive in a dynamic and fast-changing environment
• High professional integrity and healthcare ethics, with in-depth knowledge of quality and regulatory standards
• Ability to make timely, well-balanced decisions that align with compliance and business needs
• Excellent English skills are required, knowledge of German is a plus

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.