RA Market Specialist with French (all genders)

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

You role:

In this role, you will drive regulatory submission management for France, Belgium, and Luxembourg from initial planning through to final local execution. This includes managing complex dossier reviews and approvals, overseeing specialized Module 1 requirements, handling financial fee planning, and directing language-dependent activities such as localized cover letters, national Product Information, and artwork modifications. Beyond standard lifecycle management, you will actively champion early access programs (NPS/EAP) for new assets, support clinical trials, and partner cross-functionally to ensure strict quality control over all regulatory documentation and promotional materials. Ultimately, you will manage day-to-day operations and execute localized product plans that align seamlessly with broader global and regional business strategies.

Who you are:

• Hold a University degree in a scientific area.
• Possess 1 to 3 years of hands-on experience in regulatory affairs or closely related fields, such as Clinical Trials, Pharmacovigilance, or Quality Assurance.
• Familiar with the specific local regulatory frameworks, Module 1 requirements, and language compliance needs for France, Belgium, and/or Luxembourg.
• Skilled at aligning with diverse internal teams to maintain quality control, manage product plans, and support regional process initiatives.
• Proficient in English and French.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!