QA Batch Disposition Specialist III

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three RD sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a QA Batch Disposition Specialist III as part of the Quality team based in Raritan, NJ. Role Overview This exempt-level position is responsible for performing a wide range of activities to support the Manufacturing and release of CAR-T drug product for human use. This position is responsible for quality and maintaining the highest standards in compliance within company policies, procedures, and all applicable regulations. Key Responsibilities Review documentation for all manufacturing activities executed in accordance with Good Documentation Practices (GDP). Review documentation for miscellaneous activities executed in accordance with Good Documentation Practices (GDP). Work in a team based, cross-functional environment to complete tasks required to meet all business objectives. Perform regular administrative duties to maintain all manufacturing record which will involve binding and archiving and storage. Support Investigations team by providing quality and compliance input for continuous improvement and remediations; also, support or facilitate investigations for Product Quality Complaints. Review, revise, or draft Standard Operating Procedures (SOPs) in relation to the batch review/ release process. Contribute to process improvement. Ensure turnaround times are adhered to during review and disposition of the Drug Product deadlines. Perform duties/tasks under minimal direction/supervision according to standard operating and manufacturing procedures and demonstrate ability to attain resources and information from established internal contacts. Consistently perform tasks in adherence with safety policies, quality systems, and cGMP requirements, as well as according to state and federal regulatory requirements. Strive to reduce non-conformances in supported areas by dedicatedly driving compliance. Ensure readiness of manufacturing records for regulatory inspections and internal audits. Support of regulatory audits including preparation of documents, presentation to health authorities, and to lead actions in response to potential findings. Ability to utilize multiple electronic quality systems and SAP. Contribute to the improvement of QA practices to ensure accurate documentation activities, including manual and electronic practices. Collaborate with (cross)functional departments to resolve issues related to batch review/release, investigations, and receipt of QC test results to allow for timely release of final product batches according to department and business plan in a complex fast paced supply chain organization. Contribute to cross-functional projects with stakeholders to establish best practices that will reassure the target turnaround time of a CAR-T product. Requirements Bachelor’s degree required in Life Sciences or Engineering. A Minimum of 4+ years’ experience in Quality Assurance Biotech/Pharmaceutical industry experience. Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell-based products as we ... (truncated, view full listing at source)