CDMO Materials Management Senior Specialist

Role: Senior Specialist in CDMO Materials Management overseeing inventory accuracy, control, and reconciliation across radiopharmaceutical development, manufacturing, quality, and distribution functions. Objectives: ensure GMP, GDP, and regulatory compliance for radioactive, API, reagent, and finished product inventory; support uninterrupted clinical and commercial supply chains. Responsibilities: manage daily inventory control activities, including receiving, storage, cycle counting, reporting, and discrepancy investigations; maintain compliance with cGMP, radiation safety, DSCSA, DOT/IATA; lead inventory planning, SOP development, audit readiness, and cross-functional collaboration with supply chain, QA, QC, manufacturing, and vendor management. Qualifications: Bachelor’s in supply chain, life sciences, or related; 5–8+ years in regulated pharma, biotech, or radiopharmaceutical inventory roles; experience with temperature-sensitive, radioactive, or hazardous materials preferred; proficiency in ERP/WMS systems such as SAP, Oracle, PETra. Preferred skills: leadership experience, strong communication, analytical, problem-solving, and ability to operate in fast-paced environments with high compliance demands. HighValue: radiopharmaceuticals, GMP environment, regulatory compliance, inventory control, radioactive/materials management, cross-functional coordination, on-site NJ presence.