About this role
Director, Regulatory CMC at Genetix Biotherapeutics. Location: Somerville, Massachusetts, United States. Role: leading lifecycle, managing submissions, authoring documentation Requirements: 10+ years biopharma CMC regulatory experience for biologics/gene therapies; bachelor’s or master’s in life sciences; experience with post-approval CMC submissions, GMP and global regulatory frameworks; strong communication and cross-functional skills. Category: Research and Development (R&D) Seniority: Senior Level Commitment: Full Time Workplace: Hybrid Languages: English