SaMD Regulatory Affairs Lead — Global Submissions

A global health technology company is seeking a Principal Regulatory Affairs Specialist to develop regulatory strategies for new product development, focusing on Software as a Medical Device. The ideal candidate has over 7 years of experience in Regulatory Affairs and expertise in FDA and EU regulations. This role is essential in guiding cross-functional teams and communicating regulatory changes. Candidates must be located near Cambridge, MA for this office-based role. #J-18808-Ljbffr