Medical Devices Regulatory Affairs Specialist | Cambridge

Newton Colmore is seeking a Regulatory Affairs Specialist for Medical Devices in Cambridge. You will support a wide range of projects, work with engineers, scientists and designers, and help ensure compliance with global regulatory expectations across medical and non-medical sectors.

You will apply knowledge of ISO 9001, ISO 13485 and FDA 21 CFR 820, monitor regulatory changes, contribute to regulatory planning, and support audits and lifecycle management from development through commercial

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