Regulatory Affairs Cmc Specialist — Hybrid Work

Grifols is seeking a Regulatory Affairs professional in Sant Cugat del Vallès, Spain. The role focuses on preparing, reviewing, and managing complex CMC submissions to ensure timely, accurate regulatory compliance across multiple sites.You will evaluate change requests, liaise with Health Authorities, and participate in cross-functional teams for worldwide...

Position: Regulatory Affairs Biosimilar Specialist LATAM Location: Madrid Experience: 5+ years in Regulatory Affairs within innovative biopharmaceuticals and/or biosimilars Want to know more? At Exeltis, we continue to grow and we are looking for a Regulatory Affairs Biosimilar Specialist ready to take the next step in their career in an international,...

Boston Scientific is seeking a Regulatory Affairs Specialist for the EMEA region. The role focuses on coordinating regulatory activities for clinical investigations, preparing dossiers, and maintaining accurate regulatory files within a hybrid Madrid office environment.You will work with Competent Authorities, ensure timely submissions, and support safety...

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are looking for a Regulatory Affairs Specialist to join our team and...

## Regulatory Affairs SpecialistApplyremote type:Not Remotelocations:Polinyà, Spain:MERU CEDEX, France:Gdansk, Poland:Poland:Pinneberg, Germanytime type:Full timeposted on:Posted 2 Days Agotime left to apply:End Date: July 29, 2026 (18 days left to apply)job requisition id:JR8439**You Speak Up to Share Opportunities for Improvement and Drive Change? Would...

Select how often (in days) to receive an alert: Create Alert Location: in our offices in Madrid, Spain, on a hybrid working schedule (3 days per week in the office + 2 days per week working from home). About the role: The Clinical Center of Excellence (CoE) is part of the EMEA Regulatory Affairs team and provides regulatory expertise and support for...

Experteer Overview In this Regulatory Affairs Manager role, you guide complex regulatory projects and may act as a team lead or project manager under guidance. You write regulatory and technical documents with minimal supervision and manage budgets and deliverables. You engage with clients, present lessons learned, and help develop or review SOPs. You...

Regulatory Affairs Specialist, EMEA Work mode: Hybrid Onsite Location(s): Madrid, M, ES Location: in our offices in Madrid, Spain, on a hybrid working schedule (3 days per week in the office 2 days per week working from home). About the role: The Clinical Center of Excellence (Co E) is part of the EMEA Regulatory Affairs team and provides regulatory...

Regulatory Affairs Specialist, EMEA Work mode: Hybrid Onsite Location(s): Madrid, M, ES Location: in our offices in Madrid, Spain, on a hybrid working schedule (3 days per week in the office 2 days per week working from home).About the role: The Clinical Center of Excellence (CoE) is part of the EMEA Regulatory Affairs team and provides regulatory expertise...