CDMO Materials Management Manager

Role: CDMO Materials Management Manager overseeing inventory accuracy, control, and reporting across radiopharmaceutical development, manufacturing, QC, warehouse, and distribution. Responsibilities: lead daily GMP/non-GMP inventory activities, manage temperature-sensitive, radioactive, and short shelf-life materials, ensure regulatory and cGMP compliance, coordinate counts and reconciliation, support audit readiness, develop SOPs, and serve as primary contact for vendor relationships and business development within the CDMO. Requirements: Bachelor's in supply chain, logistics, life sciences, or related; 5–8 years in regulated pharma or radiopharma inventory management; leadership experience preferred; strong knowledge of cGMP, GDP, radiation safety, and inventory systems (SAP, WMS). HighValue: radiopharmaceuticals, GMP environment, radioactive and temperature-sensitive materials, regulatory compliance, cross-functional collaboration with manufacturing, QC, QA, procurement, and clients. WorkSetup: onsite in New Jersey, 5 days/week, open to U.S. applicants.