About this role
Associate Director, Drug Substance Development & Manufacturing at Entrada Therapeutics. Location: Boston, Massachusetts, United States. Role: lead development, manage batches, coordinate QA Requirements: Master’s degree in organic chemistry or related field; 8+ years pharma experience; expertise in drug substance development, GMP manufacturing, and CDMO management; travel up to 20%. Category: Engineering Seniority: Senior Level Tools: SPPS, SPOS, Lyophilization, cGMP, Process Characterization, Process Validation, CDMO Management, Regulatory Submissions, IND, NDA, IMPd Commitment: Full Time Workplace: Remote Languages: English