Aunque la experiencia cualificado y las cualificaciones son clave para este puesto, asegúrese de comprobar si posee las habilidades interpersonales preferibles antes de solicitar, si se requieren.
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- Location: Madrid
- Job type: Fixed-term, Full time
About the job
Join Sanofi's Regulatory Affairs team in Spain and play a pivotal role in bringing innovative medicines to patients while ensuring full compliance with local and EU regulatory requirements. As our Regulatory Affairs Specialist, you will act as the key liaison with Spanish and European health authorities, managing submissions and interactions with precision and timeliness. This role offers the opportunity to be a true regulatory expert — shaping submissions, safeguarding compliance, and driving impact across the full product lifecycle in a dynamic, patient-focused environment.
Join the engine of Sanofi’s mission — where deepimmunosciencemeets bold, AI-powered research. In R&D;, you’ll drive breakthroughs thatcouldturn the impossible intopossible formillions.
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
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- Ensure compliance with local and EU regulatory requirements throughout the product lifecycle
- Liaise with health authorities on submissions, requests and other interactions, ensuring timely and accurate response
- Coordinate with global/regional regulatory affairs teams to align local submissions with international regulatory strategy
- Secure optimal support to key stakeholders for on-time delivery of high quality dossiers in compliance with Health Authority requirements.
- Expertise on all dossier format
📌 Regulatory Affairs Specialist (Madrid)
🏢 Sanofi
📍 Madrid
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