About this role
Associate Director, Regulatory Affairs CMC at Voyager Therapeutics. Location: Cambridge, Massachusetts, United States. Role: Lead submissions, Prepare strategy, Coordinate submissions Requirements: 10+ years regulatory affairs experience in biotech, gene therapy; global submissions; strong FDA/health authority interaction; leadership skills. Category: Research and Development (R&D) Seniority: Senior Level Commitment: Full Time Workplace: Onsite Languages: English