Regulatory Affairs Associate - VIE Contract

About the job

Main responsibilities :

• Support the Germany, Switzerland, Austria (GSA) multi country team in life cycle management of prescription medicines and medical devices.
• Contribution to implement labelling updates.
• Preparation of variation documents for selected products.
• Database maintenance.
• Monitoring of the compliance of regulatory tools and processes.
• Management of Health Authority portal updates / reports.
• Participation in Regulatory Affairs and transversal projects.

About you

Experience :

Soft and Technical skills :

Education :

Languages :

Why choose us?

iMove is a unique program tailored for European youth interested in challenging themselves with meaningful assignments across the globe. At Sanofi we have a strong ambition to invest in young talents who will drive the success of Sanofi tomorrow.

Sanofi’s Work Abroad Program, iMove, offers jobs-assignments with actual responsibilities and a perspective to grow. We provide those opportunities in various functions such as : marketing, finance, regulatory, supply chain, clinical trials, production, etc. and in more than 40 countries. Sanofi unites people who are passionate about solving healthcare needs across the world. Joining our iMove Work Abroad Program is a unique opportunity to make a difference through your work.

LI-EUR

Pursue , discover

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 and check out our Diversity Equity and Inclusion actions at !