R&D Investigational Product Support

Regulatory Affairs Associate - VIE Contract

• Location: Vernier, Switzerland
• Target start date: 01/10/2025

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

Looking to launch your career at the cutting edge of healthcare? Join Sanofi for a chance to develop with mentoring and guidance from inspirational leaders while helping to make an impact on the lives of countless people worldwide. As Regulatory Affairs Associate VIE in our Regulatory Affairs team you will support our multi country team in life cycle management of prescription medicines and medical devices.

We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing Progress to make a real impact on millions of patients around the world.

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:

• 1+ year of experience in international and/or country regulatory affairs incl. knowledge of Swiss/European pharmaceutical regulation would be an advantage.
  

Soft and Technical skills:

• Proficiency in Microsoft Office package, has a passion for exploring digital technologies.
• Good project management and organizational skills.
• Accurate and precise working attitude.
• Strong time management and prioritization skills.
• Ability to work cooperatively with others across (multifunctional and multicultural) the organization to achieve shared objectives.
  

Education:

• Master’s degree in pharmacy or other life science discipline such as Biology, Medicine, Chemistry or related field.
  

Languages:

• Fluent English (written and verbal).
• Fluent in German.
• Fluent in French.
• Italian would be an asset.