Medtronic is seeking a QA/RA professional to support Post Market Surveillance and regulatory reporting in Colombia. You will review complaints, ensure regulatory submissions are completed on time, and collaborate with cross-functional teams to maintain quality systems.
Responsibilities include CAPA investigations, data analysis, and preparation of regulatory reports while upholding GDP, ISO 13485 and general/regional requirements. Fluent English is required.
📌 Quality System (Bogotá, D.C.)
🏢 Medtronic
📍 Bogotá, D.C.
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