Hands-On Regulatory Affairs Specialist — Medical Devices; US/EU
Position: Hands-On Regulatory Affairs Specialist — Medical Devices (US/EU)
A leading medical device company in Massachusetts is seeking a Regulatory Specialist to support regulatory activities throughout the product lifecycle. This role involves managing U.S. regulatory submissions, maintaining device registrations, and working with cross-functional teams. Ideal candidates will possess a Bachelor’s degree in a relevant field and have 1-3 years of regulatory affairs experience in medical devices. This position offers a reputed company work environment and some flexibility for remote work, making it an exciting opportunity for those early in their regulatory careers.
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