Regulatory Affairs Officer Opportunity – at Sanofi, Apply Now!
Looking to launch your international career in regulatory affairs? Sanofi, a global leader in healthcare innovation, is hiring a Regulatory Affairs Officer under its prestigious VIE Program in Amsterdam, Netherlands. This unique opportunity is open to young professionals from the European Economic Area, offering hands-on experience in global regulatory processes, drug development, and compliance within a collaborative international environment. If you’re passionate about making a difference in global health, this is your chance to join Sanofi and accelerate your career.
- Job Title: Regulatory Affairs Officer โ VIE Contract
- Location: Amsterdam, Netherlands
- Program: iMove โ International Work-Abroad Program
- Job Type: Full-Time, VIE (Volunteer for International Experience)
- Application Deadline: September 22, 2025
- Target Start Date: September 1, 2025
About The Company
Sanofi is a global healthcare leader committed to chasing the miracles of science to improve peopleโs lives. With operations in over 100 countries, Sanofi is pioneering innovations across pharmaceuticals, vaccines, and consumer healthcare. Through its iMove Program, Sanofi offers European youth the opportunity to experience international careers through challenging assignments around the globe.
About the Role
As a Regulatory Affairs Officer in Sanofiโs Global Regulatory Team, you will support global regulatory activities for drug development projects. From preparing and reviewing regulatory submissions to liaising with Health Authorities, your role will ensure timely and compliant product development that ultimately benefits patients worldwide.
Key Responsibilities
- Prepare, compile, and review documentation for submissions such as INDs, CTAs, protocols, amendments, and scientific advice.
- Coordinate with cross-functional teams and regulatory leads to ensure consistency and quality.
- Track submission progress and ensure compliance with Health Authority guidelines.
- Assist with Health Authority communications and regulatory queries.
- Utilize tools such as Veeva Vault and Plai for document and data management.
Who Should Apply?
- Sanofiโs iMove Program is open to citizens of the EEA (EU + Norway, Liechtenstein, Iceland) aged 18โ28 who are applying outside their home country. This role is ideal for early-career professionals with a background in:
- Pharmacy, Life Sciences, Biomedical, Veterinary, or Medicine
- Strong English communication and organizational skills
- Experience or interest in regulatory affairs, clinical submissions, and pharmaceutical R&D
Why Join Sanofi via iMove?
- Gain international work experience with real responsibilities
- Contribute to innovative healthcare solutions
- Work in a fast-paced, collaborative, and purpose-driven environment
- Grow professionally in one of the worldโs leading pharmaceutical companies
Ready to Chase Progress with Sanofi?
This is more than a job โ itโs a chance to shape the future of medicine. If you’re passionate about regulatory science, global collaboration, and personal growth, apply to Sanofiโs iMove Work Abroad Program today and pursue progress while discovering the extraordinary.
Keywords: Regulatory Affairs Officer, VIE Contract, Sanofi, Amsterdam, Netherlands, Job Opportunity, Global Healthcare Company, Drug Discovery, Regulatory Requirements, Regulatory Submissions
