BD is seeking a Regulatory Affairs Specialist to manage general regulatory activities for in vitro diagnostic (IVD) medical devices across the product lifecycle. You will help craft strategies, prepare registrations and ensure compliance worldwide, working with R&D;, QA, Manufacturing, and Medical Affairs.
The role requires a science background, strong regulatory knowledge, and the ability to communicate complex requirements to diverse teams.
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📌 Global IVD Regulatory Strategist (Salamanca)
🏢 BD
📍 Salamanca
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