Director, Technical (CMC) Project Management

Role: Lead CMC project management for late-stage development to commercialization and lifecycle support of small molecule medicines targeting chronic diseases, including cardiovascular, metabolic, and pulmonary conditions. Responsibilities: oversee end-to-end project planning, cross-functional coordination across drug substance, drug product, analytical, quality, regulatory, and supply chain areas; develop integrated project plans, track progress, manage risks, facilitate meetings, and coordinate with external manufacturing partners; lead budgeting, financial tracking, and reporting; establish best practices in project management within Technical Operations; serve as a strategic team member and mentor. Requirements: B.S. in Chemistry, Engineering, or related field; 12+ years in pharma/biotech CMC, with 5+ years supporting late-stage development through commercial launch; experience with small molecules and oral solid dosage products; strong understanding of manufacturing, regulatory, and supply chain processes; proficiency in project management tools (MS Project, Smartsheet, Excel, PowerPoint); proven ability to operate in fast-paced, global environments; excellent communication and cross-functional influence skills. Preferred: advanced degree (M.S. or Ph.D.) and project management certification. HighValue: leadership in CMC for late-stage pharmaceutical development, global cross-functional coordination, lifecycle management, project management excellence, up to 25% international travel.