Senior Regulatory Affairs Lead – Medical Devices (Hybrid)

A leading medical technology company is seeking a Principal Regulatory Affairs Specialist in Portage, MI. This hybrid role involves developing and implementing compliance strategies to meet global regulations in the medical device field. You will lead cross-functional teams, resolve compliance issues, and ensure integration of requirements into product development. The ideal candidate has 9+ years of experience and a Bachelor's degree in engineering or science, with a strong knowledge of FDA regulations. #J-18808-Ljbffr