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$56k – $161k per year (Estimated)
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In office (Barcelona)
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Sanofi is a French pharmaceutical company formed in 1973 and assembled over five decades through a long series of mergers including Synthelabo, Aventis and Genzyme. It is now built around immunology and rare disease, with Dupixent for atopic dermatitis and asthma as by far its largest product, alongside a substantial vaccines division covering influenza, meningitis and the respiratory syncytial virus antibody Beyfortus. Headquartered in Paris, the group has sharpened its focus in recent years by separating its consumer healthcare business into the standalone company Opella and directing research spending toward biologics and immune science.

Regulatory Promotion Specialist - VIE Contract

  • Location: Spain, Barcelona
  • Target start date: 01/11/2026

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 Promotion Specialist VIE within our Regulatory Affairs you’ll provide support on internal inquiries related to practices, materials, and collaborations.

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:

  • Collaborate in the preparation and submission of content to the relevant authorities.
  • Provide support on internal inquiries related to practices, materials, and collaborations.
  • Participate in the development and delivery of internal training sessions.
  • Update and maintain the internal repository of regulations.
  • Work collaboratively with cross-functional teams.
  • Collaborate and participate in the annual meeting with health authorities.

About you

Experience:

  • Previous experience in Regulatory Affairs would be an asset.

Soft and technical skills:

  • Ability to interpret and apply regulatory guidelines and legislation.
  • Problem-solving capabilities - able to assess regulatory challenges and propose effective solutions.
  • Strong team spirit and ability to collaborate across departments.
  • Proactive and accountable mindset.
  • Analytical Thinking and problem-solving orientation.
  • Ability to manage priorities and respond to urgency.
  • Excellent organizational skills and attention to detail.
  • Quick Learner, able to grasp new concepts and frameworks.
  • High level of Integrity and professionalism.
  • Strong communication and diplomatic skills.
  • Openness to change and continuous improvement.
  • Results-driven approach.

Education:

  • Bachelor’s or master’s degree in pharmacy or a related field.

Languages:

  • Fluent English (written and verbal).
  • Spanish B2 level.

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.

#LI-EUR

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!

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