About this role
Senior International Regulatory Affairs Specialist at Butterfly Network. Location: Burlington or New York City. Role: Coordinate submissions, Maintain registrations, Assess impact Requirements: 5+ years regulatory affairs in medical devices; SiMD/SaMD; global submissions; EU MDR 2017/745; ISO 13485/14971; strong English. Category: Research and Development (R&D) Seniority: Senior Level Tools: Document management systems, Regulatory submission platforms, Quality Management System (QMS) Commitment: Full Time Workplace: Hybrid Languages: English