About this role
Associate Director, Drug Substance & Manufacturing (Late-Stage) at Rapport Therapeutics. Location: Boston, Massachusetts, United States. Role: supporting lifecycle, designing DoE, managing CDMOs Requirements: M.S. or Ph.D. in Process/Organic Chemistry or Chemical Engineering; 8+ years (Ph.D.) or 10+ years (M.S.) in small-molecule drug substance development; experience with DoE, CPV, CDMOs, and ICH guidance for late-stage/registration. Category: Research and Development (R&D) Seniority: Senior Level Tools: DoE, CPV, ICH Q7-Q12, ICH Q3A, ICH Q3C, ICH Q3D, ICH M7, NDA, MAA Commitment: Full Time Workplace: Hybrid Languages: English