Medical Device Risk Manager
Listed on 2026-10-11
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Management
Regulatory Compliance Specialist
Sinclair Group in the United States is seeking a Risk Manager to oversee risk management for medical devices and aesthetic products, reporting to the R&D Director. You will ensure compliance with ISO 14971, ISO 13485, MDR, and Annex XVI across development and legacy devices.
The role requires at least 2 years in regulated medical devices, knowledge of usability engineering, and strong risk assessment skills. Fluent English is essential, and a Master’s in engineering is preferred.
This posting is for the Medical Device Risk Manager role at Sinclair Group, based in Town of Poland, NY, United States.
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We are looking to fill the Medical Device Risk Manager position at Sinclair Group in Town of Poland, NY, United States.
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