MSAT Head - Gödöllő Site

As the MSAT Head for the Gödöllő site, you will provide scientific and technical leadership to ensure robust, compliant and continuously improving manufacturing processes.

You will oversee Manufacturing Support, Validation and the Process Development Laboratory while guiding investigations, process optimization and lifecycle management. You will drive process science and technology initiatives, ensure the validated state of GMP systems and enable strong collaboration with site and global MSAT teams.

Your leadership supports inspection readiness, quality performance and strategic decision-making as an active member of the Site Leadership Team.

Key Responsibilities:

• Lead MSAT teams including Manufacturing Support, Validation and the Process Development Lab.

• Ensure CPV, process stewardship, validation planning and GMP compliance.

• Oversee technical transfers, process optimization projects and technology benchmarking.

• Support quality events, RCA, CAPA and inspection readiness.

• Drive EHS performance and continuous improvement across MSAT.

Basic Qualifications & Skills:

• Proven experience in pharmaceutical manufacturing leadership, preferable within vaccines, biologics, or other highly regulated production environments.

• Strong knowledge of cGMP, quality systems, regulatory expectations, and biological production processes.

• Demonstrated capability in people management and organizational development.

• Fluent written and spoken English.

• Excellent communication, problem-solving, and decision-making skills.

Preferred Qualifications & Skills:

• Experience with vaccine or biological product manufacturing.

• Technical transfer experience including third-party transfers.

• Knowledge of process characterization and validation strategies.

• Experience leading cross-functional improvement programs.

• Business English; Hungarian language an advantage.

Work Pattern:

• Full-time on-site leadership position with presence required on site with hybrid set-up

• Occasional extended-hours availability depending on operational needs, audits, or critical events.

• High visibility role with significant responsibility for people, quality, safety, and business performance.

Please note that relocation package cannot be provided for this role.

#LI-Hybrid

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

Should you require any specific adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on hu-inclusion.recruitment@gsk.com.

Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels’.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

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