Strategic Regulatory Lead — Medical Devices

A leading medical device company in Manchester, NH is seeking a Regulatory Affairs Project Manager. The role involves defining and executing regulatory strategies for FDA approval of innovative life science devices, mentoring staff, and leading FDA interactions. Candidates should have a BS in a related field and a minimum of 5 years' experience in medical device regulations. The position offers the opportunity to contribute to meaningful projects in an innovative and fast-paced environment.
#J-18808-Ljbffr