Regulatory Affairs Officer - VIE Contract

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.

Ready to get started?

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 (GSS).
• Participate in the preparation of consultations with authorities
• Support the GRL for the meetings of the product regulatory team (GRT) composed of the different regulatory experts (Regulatory CMC, Regulatory Labeling, Regional Regulatory contacts, Regulatory Operations): preparation, meeting minutes, follow-up of actions.
• Support the Global Regulatory Lead (GRL) for the update of the document summarizing the Global Regulatory Product Strategy (GRPS).
• Support the local regulatory team in all relevant regulatory activities.

About you

Experience:

• 1-2 years of experience in pharmaceutical regulatory affairs or significant internship in the field.
• Experience in an international environment is appreciated.

Soft and technical skills:

• Knowledge of pharmaceutical regulations & registration dossiers.
• Understanding of regulatory submission processes, analytical and writing competencies
• Strong AI skills and practical experience are desirable.
• Ability to work autonomously.
• Rrigor and adaptability.
• Strong intercultural communication, teamwork skills.
• Strong written and verbal communication abilities.

Education:

• Master's degree in Pharmacy, Pharmaceutical Sciences, Regulatory Affairs or related scientific field (Chemistry, Biology, Biotechnology).

Languages:

• Fluent English (written and verbal).

Why choose us?

• Be part of a pioneering biopharma company where patient insights shape drug development.
• Work at the forefront of AI-powered science that accelerates discovery and improves outcomes.
• Collaborate beyond your expertise, sparking new ideas with diverse, multidisciplinary teams.
• Help improve the lives of millions of people globally by making drug development quicker and more effective. 
• Enjoy opportunities to collaborate beyond your area of expertise, working with diverse teams across science, clinical, and digital fields to spark new ideas and drive breakthroughs. 
• Join a workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice.
• Achieve genuine work-life balance in a supportive R&D environment.

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. 

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