Associate Director, CMC Project Management

Role: Lead CMC Program Management for biopharma development, focusing on strategic execution of manufacturing, supply chain, and regulatory activities to ensure timely clinical progression and commercialization of oncology therapies. Responsibilities: develop and oversee integrated cross-functional plans, manage budgets and financial planning, establish and monitor external manufacturing partnerships (CMOs/CDMOs), and provide program governance and risk mitigation. Qualifications: advanced degree in Chemical Engineering, Pharma Sciences, Chemistry or related field; 9+ years in biopharma CMC development, with proven experience in program leadership, NDA filing, and product launch. Skills: deep expertise in CMC, strong leadership in matrixed teams, extensive CMO/CDMO management, financial acumen, and excellent communication. High-Value: focus on oncology, biologics or small molecules, late-stage development, regulatory filings, global supply chain, and external manufacturing oversight. WorkSetup: on-site in South San Francisco; salary range $210,000-$240,000; not H-1B eligible.