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QA Investigations Lead responsible for quality oversight in producing personalized cell therapy, ensuring compliance, managing investigations, and tracking metrics in a sterile GMP environment. Collaborates with teams, reviews procedures, and supports regulatory inspections. Requires Bachelor's Degree and 4 years of relevant experience in aseptic manufacturing facility.

The Operations Supervisor at Legend Biotech leads daily production operations in a cGMP environment, supervising multiple units within the CAR-T process. Responsibilities include conducting operational meetings, guiding production personnel, managing change controls, supporting manufacturing investigations, and collaborating with cross-functional teams to enhance production efficiency and compliance.

The CAR-T Batch Logistics Planner will manage the efficient release of patient-specific drug product batches by coordinating with cross-functional teams. Key responsibilities include overseeing batch release processes, resolving issues, and fostering communication among stakeholders to enhance operational efficiency.