Becton Dickinson is seeking a Regulatory Affairs Specialist to contribute to regulatory strategy and submission activities for medical devices. The role focuses on MDR compliance, international registrations, and maintaining technical documentation throughout the product life-cycle.You will lead regulatory assessments, support audits by authorities, and collaborate with cross-functional teams to ensure timely approvals and certifications across markets.#J-18808-Ljbffr
📌 Global Regulatory Affairs Specialist Medical Devices (Madrid)
🏢 Becton Dickinson
📍 Madrid
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