Regulatory Planner VIE Contract

Regulatory Planner- VIE Contract

• Location:United States of America, Swiftwater
• Target start date: 01/12/2026

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 Planner VIE within our Research & Development (R&D) team you will enable the Regulatory team and GRA to rapidly develop and implement the right solutions. This role is essential to advancing our capacity management initiatives, ensuring agile response to business priorities and fostering a data-driven approach to decision-making.

Join the team protecting half a billion lives every year with next-gen science, mRNA innovation, and AI-driven breakthroughs. In Vaccines, you’ll help advance prevention on a global scale - and shape the future of immunization.

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:

• Owner of the operational planning of several Pharma & Vaccines projects for all regulatory activities whatever their location. 
• Ensures the project strategy is reflected in terms of Planning into the operational plan. Is accountable for the customization of the operational plan with the most known information.  
• Supports impact management by making analyses and assessing planning scenarios with project and planning actors. 
• Communicates the updates to the appropriate stakeholders as well as any report (Gantt chart) supporting decision management. 
• Revamps the template documentation in a comprehensive way & agile way, adapting to template evolution.
• Documentation in a comprehensive way & agile way, adapting to template evolution.
• Participates in any user requirement definition &/or testing for new reports & upgrades of existing ones.

About you

Experience:

• General knowledge on overall R&D Drug Development and good knowledge in Business operational activities (Regulatory).

Soft and technical skills:

• Good knowledge of Project Management.
• Strong knowledge in planning management.
• Rigor, Analytical skills and spirit of synthesis, Quality orientation.
• Excellent organizational skills, rigor, striving for results, high accuracy orientated.
• Strong communication skills and interpersonal relationship demonstrated.
• Excellent presentation skills (verbal and written).
• Strong Networking skills.
• Creative problem-solving skills.
• Good computers skills.
• Knowledge of planning tool (Gantt chart).

Education:

• Master’s degree in a scientific degree and / or regulatory affairs.

Languages:

• Fluent in English (verbal and writing).

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. 
• Share knowledge with leading scientists, engineers, and experts in a purpose-driven community dedicated to protecting millions worldwide. 
• Be part of a company that believes in the future with significant investment annually in manufacturing innovation. 
• Help create sustainable vaccine solutions, from reducing carbon emissions in production to increasing global access to life-saving immunizations. 
• Gain hands-on experience in state-of-the-art digital and AI-powered manufacturing facilities, where you can be part of industry-leading advancements.
  

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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