Regulatory Affairs Specialist
Roche · Sant Cugat del Vallès
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- Company
- Roche
- Location
- Sant Cugat del Vallès
- Employment type
- Full-time
- Posted
- October 1, 2026
About this job
As a Regulatory Affairs Specialist you will have the opportunity to work with internal and external teams for project/product realization, write and prepare submission packets for health authority marketing approvals, and utilize agile principles to drive regulatory activities for our Oncology In-vitro Diagnostics (IVD) team. Your Opportunity Regulatory document and submission compilation: You oversee the development of registration dossiers for moderately complex products or programs. You develop and manage comprehensive global regulatory submissions and registration plans. External interface management: You take initiative and partner effectively with stakeholders to understand problems and opportunities to provide best solutions.…
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