Senior Regulatory Affairs & Quality Lead - MedTech (Hybrid)

A leading medical technology company is seeking a Senior Specialist, Regulatory Affairs & Quality in Markham, ON. The role involves developing and executing regulatory strategies for Class III and IV medical devices, managing all product lifecycle regulatory aspects, and providing expert guidance to teams. With a focus on compliance and quality improvement, candidates should have at least five years of experience in regulatory affairs within the medical device sector. This position supports a Flex / Hybrid work schedule and is a 12-month fixed-term role.

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