BD in Spain is seeking a Regulatory Affairs Specialist to guide regulatory activities across product development and commercialization. You will ensure compliance with MDR, prepare and maintain Technical Files, and manage international registrations in a fast-evolving general environment.
Expect collaboration with cross-functional teams, audits by authorities, and contribution to product life-cycle regulatory tasks.
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📌 Medtech regulatory lead — global compliance & dossiers (Comunidad de Madrid)
🏢 BD
📍 Comunidad de Madrid
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