Global Regulatory Affairs Lead: Medical Devices & SaMD

A leading medical device company in North Carolina, is seeking a Regulatory Affairs Specialist who will oversee regulatory activities for medical devices and Software as Medical Device (SaMD). The role includes leading global assessments and managing submissions for regulatory approvals and compliance. Candidates should have at least 2 years of experience in regulatory affairs within the industry, a Bachelor’s degree in a related field, and strong communication skills. This position offers opportunities for professional growth in a dynamic environment. #J-18808-Ljbffr