About this role
Principal Scientist, Regulatory Strategy at Kymanox. Location: United States. Role: Lead submissions, Attend meetings, Review data Requirements: 7+ years regulatory experience in US medical devices/pharma; 2+ years in leadership; US FDA/EU submissions; QMS knowledge; eCTD publishing; regulatory strategy and risk assessment. Category: Legal and Compliance Seniority: Senior Level Tools: eCTD, Regulatory submissions, FDA, EMA, Quality System, ISO 13485 Commitment: Full Time Workplace: Onsite Languages: English