Follow up on inspection observations and corrective and preventive actions (CAPAs) to ensure timely closure.
Liaise with local health authorities regarding quality-related regulatory requests and commitments.
Serve as backup for Annual Product Quality Review (APQR) activities.
About you
Experience: Background in pharmaceutical quality assurance, quality control, or regulatory affairs(2-5 years of relevant experience required)
Soft and technical skills: Strong attention to detail, analytical thinking, and familiarity with GxP quality systems and complaint/deviation handling processes; able to work independently and collaboratively across cross-functional teams
Education: Degree in Pharmacy, Chemistry, Life Sciences, or a related field
Languages: Professional proficiency in English for collaboration with global teams
Why choose us?
Help shape the future of care for chronic and complex conditions like aT1D, Type 2 diabetes, transplant, and cardiovascular disease.
Drive meaningful impact at global scale: our medicines reach more than 100 million people each year.
Be part of a simpler, digital- and AI-powered business that’s rethinking how we work and engage with the world.
Turn bold ideas into breakthrough launches, with multiple new therapies planned through 2030 and beyond.
Stretch your career in a development playground, with opportunities across functions, regions, and the entire product lifecycle.
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!