Michael Page Colombia seeks a Regulatory Affairs & Technical Director for a medical devices-focused organization in Bogota. You will oversee regulatory compliance, quality systems, and post-market activities, coordinating with manufacturers and health authorities to ensure continuous registration and safe product performance.
The role requires completion of relevant degrees and a minimum of five years in regulatory affairs or QA within medical devices, with strong knowledge of INVIMA procedures
📌 Senior Regulatory Affairs Lead — Medical Devices (Bogotá, D.C.)
🏢 Michael Page Colombia
📍 Bogotá, D.C.
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