Global Medical Device Regulatory Affairs Strategist

A leading healthcare company is seeking a skilled Medical Device Regulatory Affairs Specialist in Annapolis, Maryland. The successful candidate will drive regulatory strategies for AI-enabled software products, ensuring compliance with evolving laws. Responsibilities encompass evaluating internal operations, coordinating regulatory submissions, and conducting audits. Applicants should have at least 6 years in regulatory affairs, preferably within med-tech, and must be adept at navigating complex regulations. Comprehensive benefits and a competitive salary range from $87,000 to $178,100 annually are offered. #J-18808-Ljbffr