Regulatory Affairs Associate - VIE Contract

• Location: Austria, Vienna
• Target start date: 01/12/2025

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 local regulatory affairs including knowledge of EU regulations 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.
• French & Italian would be an asset.

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!

Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.

With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting www.sanofi.com or via our movie We are Sanofi