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
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📌 Senior Regulatory Affairs Lead — Medical Devices (Invima) (Bogotá)
🏢 Michael Page Colombia
📍 Bogotá
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