Location: Miskolc, HungaryJob type: Permanent, Full time

About the job

As Qualification and Validation Manager within our Manufacturing & Supply team in Csanyik, you'll lead critical quality assurance activities ensuring compliance and excellence in our pharmaceutical manufacturing processes. Ready to get started?

Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you'll help reimagine how life-changing treatments reach people everywhere, faster.

About Sanofi:

We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.

Main responsibilities:

Implement and maintain qualification and validation strategies, plans, protocols, and reports in collaboration with internal and external stakeholdersEnsure compliance of qualification and validation activities with regulatory requirements and company quality standardsMaintain systems to properly identify, track, and mitigate compliance and quality risksOversee the execution of process / product validation and qualification for equipment, facilities, and systemsEstablish metrics and KPIs to monitor validation activities, identify trends and conduct periodic reviewsLead and manage the qualification and validation team, including hiring, training, coaching, and performance evaluationParticipate in regulatory inspections and audits, providing quality validation support to site experts

About you

Experience in validation and qualification activities within pharmaceutical or biotechnology industry will be preferredExperience as Quality Assurance, Quality Control and similarEducation: Master degree: pharmacist, chemist, biologist, mechanical engineer will be preferredTechnical skills: Proven experience managing qualification and validation projects, including planning, execution, and documentationSoft skills: Strong understanding of regulatory requirements (FDA, EMA), excellent communication skills, ability to manage multiple projects simultaneouslyLanguages: Fluent in Hungarian and English

Why choose us?

Shape the future of medicine delivery with cutting-edge technology and AI-driven innovationDevelop new skills, explore cross-functional roles, and work in an environment that values growth and discovery.Be part of an organization that invests in people, technology, and sustainability, leading the industry in low-carbon manufacturing and digital transformation.Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impactTake good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave

#LI-EUR

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!