Regulatory Affairs Officer - VIE Contract
About this role
Regulatory Affairs Officer - VIE Contract Location: Finland, Espoo
Target start date: 01/09/2026
iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.
PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.
PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. Please make sure to apply with your personal email address.
About the job
As Regulatory Affairs Officer VIE within our Regulatory Affairs team, you will work within the Global Regulatory Affairs Department of the Sanofi Vaccines unit, participating in the missions of the Global Regulatory Affairs Traveler Endemic Vaccines Team. Locally you will work within the Finnish Regulatory Team, conducting regulatory activities for the affiliate.
Join the engine of Sanofi's mission - where deep immunoscience meets bold, AI-powered research. In R&D, you'll drive breakthroughs that could turn the impossible into possible for millions.
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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:Coordinate of regulatory activities to support the product lifecycle or development plans and support the CTD task force. Coordinate of regulatory activities to support the Global Submission Plan with the global product regulatory team (GRT), track and update Global Simultaneous Submission plan (G