Specialist, CAR T Production Planning and Scheduling

Role: Specialist in CAR T production planning and scheduling, responsible for inventory verification, regulatory compliance reporting, and supplier material management. Objectives include ensuring accurate inventory records, compliance with laws and policies, and effective supplier performance tracking. Responsibilities encompass preparing regulatory reports, maintaining transaction records, generating delivery schedules, and evaluating supplier metrics. Requirements: Bachelor’s degree, experience in biopharma manufacturing or supply chain, strong understanding of regulatory and GxP standards. Preferred skills include experience with cell/gene therapy modalities, especially CAR T manufacturing, and familiarity with production scheduling systems. High-value specifics: focus on cell/gene therapy, post-IND or clinical stage manufacturing, regulatory compliance, and material traceability. Collaboration involves cross-functional teams in manufacturing, quality, and supply chain. Work setup: onsite in Summit West, NJ, with possible flexibility; no travel specified.