About this role
Director, Regulatory & Clinical Affairs at Nova Biomedical Corporation. Location: Waltham, Massachusetts, United States. Role: Lead strategy, Prepare submissions, Interface FDA Requirements: Lead regulatory and clinical affairs; 5–15+ years in Medical Device/IVD; regulatory submissions; ISO 13485; FDA/ international reg knowledge; strong writing/communication; travel. Category: Quality Assurance Seniority: Senior Level Tools: Microsoft Word, PowerPoint, Regulatory Submissions Commitment: Full Time Workplace: Hybrid Languages: English