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The QC Investigations Specialist will lead investigations related to laboratory deviations and corrective actions in a GMP environment. Responsibilities include interviewing personnel, reviewing CAR-T manufacturing nonconformance investigations, collaborating on improvement initiatives, monitoring metrics, and ensuring compliance with quality and safety standards.

Supervisor, QC Microbiology role at Legend Biotech in Raritan, NJ, overseeing routine Environmental Monitoring sampling in a controlled GMP environment for cell therapy products. Responsible for creating/approving QC documents, maintaining microbiological control strategy, and training on aseptic techniques.

The Financial Analyst will be responsible for reporting, forecasting, and budgeting for the CARVYKTI manufacturing program. They will develop financial models and work closely with various functional areas.