PQE Group is seeking experienced Design Controls and DHF Remediation Specialists to support medical device manufacturers with quality system and product lifecycle compliance initiatives. The successful candidate will serve as a subject matter expert in Design Controls, Risk Management, Design Assurance, and Quality Systems.
They will lead remediation and reconstruction of DHF, Technical Documentation, and related records to ensure FDA, ISO 13485, MDR/IVDR compliance, requiring strong technical
📌 DHF Remediation Specialist — Medical Devices (Ciudad de México)
🏢 Pqe Group
📍 Ciudad de México
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