Regulatory Affairs Job at Sanofi, Finland | Life Sciences | Apply Now
If you are a young European professional looking to launch a transformative international career in biopharma, this Regulatory Affairs Officer (VIE Contract) at Sanofi is a spectacular opportunity. Located in Espoo, Finland, this role bridges global vaccine strategy with local regulatory execution. For candidates eager to step into a high-impact Regulatory Affairs Job while building a long-term Sanofi career, the iMove VIE program offers a structured, prestigious pathway. If you are ready to embrace a highly dynamic Job in Finland, here is a complete, scannable breakdown of the role, your responsibilities, and the specific program qualifications required.
- Job Position: Regulatory Affairs Officer – VIE Contract
- Location: Espoo, Finland
About The Company
Sanofi is a global, R&D-driven, AI-powered biopharmaceutical company committed to improving people’s lives and delivering compelling growth. With a deep understanding of the human immune system, Sanofi invents medicines and vaccines that treat and protect millions worldwide.
What is the iMove VIE Program?
iMove is Sanofi’s premier Work Abroad Program, specifically tailored for European youth. It provides real job assignments with actual responsibilities and a clear perspective to grow into future leadership roles. By joining iMove, you are not just landing a job; you are starting a journey surrounded by mentors who challenge and inspire you to explore the intersection of science, digital innovation, and business.
Key Responsibilities
As a Regulatory Affairs Officer within the Global Regulatory Affairs Department of the Sanofi Vaccines unit, you will participate in the missions of the Global Regulatory Affairs Traveler Endemic Vaccines Team, while locally executing regulatory activities for the Finnish affiliate.
Your day-to-day strategic and operational duties will include:
- Lifecycle Coordination: Coordinating regulatory activities to support the product lifecycle and development plans, while actively supporting the Common Technical Document (CTD) task force.
- Submission Planning: Coordinating regulatory activities to support the Global Submission Plan alongside the Global Regulatory Team (GRT). You will track and actively update the Global Simultaneous Submission (GSS) plan.
- Authority Consultations: Participating directly in the preparation of official consultations with regional and global health authorities.
- GRT Management: Supporting the Global Regulatory Lead (GRL) during GRT meetings (which include experts in CMC, Labeling, and Regulatory Operations). This includes meeting preparation, minute-taking, and tracking action follow-ups.
- Strategy Documentation: Assisting the GRL in updating the core document summarizing the Global Regulatory Product Strategy (GRPS).
- Local Support: Supporting the local Finnish regulatory team in all relevant, day-to-day affiliate regulatory activities.
Qualifications & Skills Required For Regulatory Affairs Job
Important Note: Because this is a VIE program, specific age and citizenship requirements strictly apply.
VIE Program Eligibility:
- You must be a citizen of the European Economic Area (EU + Norway, Liechtenstein, and Iceland).
- You must be aged between 18 and 28 years old.
- CRITICAL: You cannot apply to a VIE assignment in your own country of citizenship (i.e., Finnish citizens cannot apply for this specific role in Espoo).
Education & Experience:
- Education: A Master’s degree in Regulatory Affairs, or a related scientific field (e.g., Biology, Biotechnology).
- Experience: 1 to 2 years of professional experience in pharmaceutical regulatory affairs, or a highly significant internship in the field. Prior experience in an international environment is deeply appreciated.
- Language: Fluent English (both written and verbal) is strictly required. (Applications submitted only in French will not be considered).
Technical & Soft Skills:
- Strong knowledge of pharmaceutical regulations, registration dossiers, and submission processes.
- Excellent analytical and scientific writing competencies.
- AI Proficiency: Strong AI skills and practical experience utilizing AI-powered tools are highly desirable.
- Work Style: The ability to work autonomously with rigor and adaptability, paired with strong intercultural communication and teamwork skills.
In summary, this Regulatory Affairs Officer VIE contract in Espoo is a highly prestigious launchpad for European youth wanting to master international drug and vaccine compliance. Securing this Regulatory Affairs Job allows you to leverage your Master’s degree to coordinate global submission strategies alongside industry leaders. If you meet the VIE eligibility criteria and are ready to chase the miracles of science, apply today to secure this unique Job in Finland and fast-track your global Sanofi career.
