About this role
Associate Director, Analytical Development and Quality Control at Kailera Therapeutics, Inc.. Location: Waltham, Massachusetts, United States. Role: supporting development, authoring documents, overseeing transfers Requirements: Advanced analytical development and QC experience for peptide therapeutics; knowledge of cGMP, regulatory filings (IND/NDA/MAA), CDMO oversight, and strong written/verbal communication. Category: Research and Development (R&D) Seniority: Senior Level Commitment: Full Time Workplace: Hybrid Languages: English