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 integral environment.Expect collaboration with cross-functional teams, audits by authorities, and contribution to product life-cycle regulatory tasks.#J-18808-Ljbffr
📌 Medtech Regulatory Lead — Global Compliance & Dossiers (Madrid)
🏢 BD
📍 Madrid
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