Cutera, based in Raleigh, NC, seeks a Senior Manager, Regulatory Affairs to lead global regulatory activities for FDA Class II and EU MDR Class IIb devices. You will shape regulatory strategies, guide lifecycle management, and manage complex submissions across international markets.

Ideal candidate has 8–12 years in medical device regulatory affairs, strong writing and cross-functional collaboration skills, and a track record of leading global regulatory programs with multi-market experience.