Senior Manager, PharmSci Clinical Manufacturing Planning

Role: Senior Manager within Takeda's Strategic Planning Group in PharmSci Clinical Manufacturing Planning, responsible for developing and executing risk-aware, program-level production plans for Drug Substance (DS) and Drug Product (DP) across clinical portfolios. Responsibilities: translate cross-functional inputs into feasible, risk-managed plans; develop alternative scenarios; identify and mitigate supply risks; align stakeholders (CMC, vendors, GCSC); prepare governance materials; monitor plan execution; drive process improvements. Requirements: Bachelor's in Life Sciences, Engineering, Supply Chain or related; 6+ years in pharma/biotech supply chain planning, CMC, or manufacturing; experience managing production and demand/supply balancing in regulated environments; strong analytical, stakeholder engagement, communication, and GxP knowledge; certifications like APICS, PMP preferred. HighValue: clinical stage (Phases 1-3), focus on supply continuity, cross-functional collaboration, risk mitigation, process optimization, and GxP compliance. Location: Lexington, MA. Work setup: full-time, on-site. No travel specified.