Associate Scientific Director, Synthetic Molecule DS Project Lead

Role: Associate Scientific Director, Synthetic Molecule DS Project Lead within Pharmaceutical Sciences, responsible for leading late-stage synthetic molecule development and process validation (PV). Objectives: ensure phase-appropriate strategy, high-quality execution, and risk management for drug substance programs, fostering cross-functional collaboration and talent development. Responsibilities: provide leadership for drug substance and PV activities, integrate program resources, ensure application of QbD principles, manage risks/issues, and contribute to process and operating model improvements. Requirements: Bachelor's, Master's, or PhD with 7+ to 15+ years' industry experience; proven expertise in synthetic small molecule DS process development, late-stage development, cGMP manufacturing, and regulatory support (IND/CTA/NDA). Skills: strong technical troubleshooting, matrix leadership, GMP documentation, excellent communication, risk management, and digital fluency, including AI tool use. High-value: focus on synthetic small molecule drugs, late-stage development, process validation, cross-functional leadership, regulatory interactions, and external partner oversight. Location: Cambridge, MA (Hybrid).