Risk Manager, Medical Devices | MDR Focus
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Sinclair is seeking a Risk Manager to lead risk management across development and legacy devices in our Lyon, France facility. You will ensure adherence to ISO 14971, MDR, and regulatory requirements while collaborating with Human Factors and cross-functional teams to maintain patient and user safety.
The role requires at least 2 years in regulated medical devices, expertise in usability engineering and risk assessment, and a Master’s in Engineering.