Specialist, CAR T Production Planning and Scheduling

Role: CAR T Production Planning and Scheduling Specialist responsible for inventory verification, regulatory compliance reporting, and material management activities in biopharma manufacturing. Responsibilities include preparing compliance reports, managing supplier delivery schedules, maintaining accurate transaction records, and evaluating supplier performance metrics. Requirements: relevant degree, experience in biopharma production, inventory management, or supply chain, with familiarity in regulatory standards and compliance documentation. Preferred qualifications: experience with CAR T therapies or cell/gene modalities, knowledge of GMP regulations, and proficiency in material traceability systems. High-value specifics: focus on biopharma manufacturing, inventory oversight, regulatory reporting, and supplier coordination within a biotech or pharmaceutical setting. Work setup: not explicitly stated, but likely on-site based on manufacturing context.