Director, Drug Product Formulations

Role: Lead global formulation strategy and execution for oral drug products from early development through commercialization, focusing on scalable, phase-appropriate solid dosage formulations. Responsibilities: oversee drug product design, develop robust formulations using QbD principles, manage process development and scale-up, direct technology transfer, ensure regulatory compliance through high-quality CMC submissions, establish platform formulation strategies, and manage external manufacturing partnerships. Collaborate with cross-functional teams including Analytical, Regulatory, Quality, Supply Chain, and Commercial, supporting early-stage development and lifecycle management. Qualifications: PhD or MS in Pharmaceutical Sciences, Chemical Engineering, Chemistry, or related field; 10+ years in drug product development and manufacturing within pharma/biotech, with leadership experience. High-value: expertise in oral solid dosage forms, enabling technologies, BCS class II/IV drugs, process validation, and global GMP/regulatory standards. Location: Boston-based, hybrid work model; some travel expected.