Sanofi
About the job
As a Regulatory Affairs Intern, you will join Sanofi's Global Regulatory Affairs team, supporting regulatory activities for medicines in the Rare Diseases and Rare Blood Disorders portfolio, including both marketed products and those in development.
Working alongside experienced regulatory professionals, you will gain hands-on experience in global regulatory processes, contribute to regulatory submissions, and support activities that help bring innovative treatments to patients worldwide.
Ready to grow your skills while helping shape the future of healthcare? At Sanofi, you’ll be empowered to learn, ask questions, and bring your ideas to life – all while supported by inspiring mentors and collaborative teams.
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:
About you
To excel in this role you will need to have:
Why choose us?
We reserve the right to close this vacancy earlier than the advertised closing date should we receive a sufficient number of applications.
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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!