Company Profile

Legend Biotech USA

Company Overview

Legend Biotech is a global clinical-stage biopharmaceutical company engaged in the discovery and development of novel cell therapies for oncology and other indications. Our team of over 1,000 employees across the United States, China and Europe, along with our differentiated technology, global development, and manufacturing strategies and expertise, provide us with the strong potential to discover, develop, and manufacture cutting edge cell therapies for patients in need.

Company History

Legend Biotech was founded as an early-stage cell therapy company in 2014. The company was the brainchild of visionary scientists who recognized that antibody-based therapeutics could potentially treat disease and possessed the backgrounds in immunology and gene editing to take the leap.

For two years, Legend Biotech, then known as the “Legend Project,” operated in a room the size of a freight elevator, with the goal of creating a cell therapy for multiple myeloma, a hematological cancer that often relapses and can become refractory. The team produced nanobodies for single-domain antibody drugs and ultimately extended the half-life of the nanobodies with proprietary technologies.

In 2015, Legend’s scientists focused on research for chimeric antigen-receptor T-cells (CAR-T) targeting the BCMA protein, making the biotech one of the first companies in the world to engineer CAR-T cells for the BCMA protein. In 2016, investigator-initiated trials began in China.

In 2017, data from the trials were presented at the American Society for Clinical Oncology (ASCO), which led to a partnership with biopharmaceutical company Janssen Biotech, Inc. to co-develop the anti-BCMA CAR-T, ciltacabtagene autoleucel (cilta-cel). Applications seeking approval of cilta-cel for the treatment of patients with RRMM are currently under regulatory review by several health authorities around the world. CARVYKTI™ (ciltacabtagene autoleucel) was approved by the U.S. Food and Drug Administration in February 2022 and received conditional marketing approval from the European Medicines Agency in May 2022.

Today Legend Biotech is a global, commercial-stage company driven by a passion for patients. We continue to build our pipeline of cell therapy platforms, which includes CAR-T, CAR-NK, CAR-?? T and non-gene-editing CAR technologies.

Our goal is to bring hope and opportunity to patients and their families by continuing to explore unique technologies.

Positions Available
  • 2 days ago

    Associate Director, CMC Project Management

    Legend Biotech USA - Somerset, NJ, United States

    Legend Biotech is seeking an Associate Director, CMC Project Management as part of the Technical Development team based in Somerset, NJ.Role OverviewThe Technical Project Manager role will support/lead CMC drug development activities for clinical pipeline programs. The PM will be responsible for the coordination of technical projects, including successful planning and execution of CMC program deliverables as well as oversight throughout entire execution to ensure success as defined by adherence ...

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  • 4 days ago

    Manager, Site Indirect Procurement

    Legend Biotech USA - Raritan, NJ, United States

    Legend Biotech is seeking Manager, Site Indirect Procurementas part of the Supply Chain team based in Raritan, NJ. Role OverviewThe Manager, Site Indirect Procurement, will be responsible for supporting and executing all Indirect Procurement activities at the commercial CAR-T cell therapy manufacturing site. This includes procurement of materials, services, equipment and capital expenditures (CapEx), ensuring alignment with business objectives, quality, compliance, and cost optimization. The ...

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  • 4 days ago

    QA Investigations Lead III

    Legend Biotech USA - Raritan, NJ, United States

    Legend Biotech is seeking QA Investigations Lead III as part of the Quality team based in Raritan, NJ. Role OverviewThe QA Investigations Lead is responsible for providing quality oversight over the production of a personalized cell therapy to support both clinical and commercial requirements in a sterile GMP environment. This includes supporting and approving manufacturing investigations, ownership of various department projects, and tracking of quality metrics while ensuring high quality ...

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  • 7 days ago

    Operations Process Trainer

    Legend Biotech USA - Raritan, NJ, United States

    Legend Biotech is seeking an Operations Process Trainer as part of the Technical Operations team based in Raritan, NJ. Role OverviewThe Operations Process Trainer will be responsible for performing training activities for Operations team members who support cGMP Clinical and Commercial Cell Therapy Manufacturing. This individual will partner with Training team members in collaboration with management in Operations to support personalized cell therapy production through safe and compliant operations ...

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  • 8 days ago

    Sr. QA Validation Specialist, CSV & Equipment

    Legend Biotech USA - Raritan, NJ, United States

    Legend Biotech is seeking a Sr. QA Validation Specialist, CSV & Equipmentas part of the Quality team based in Raritan, NJ. Role OverviewThe Sr. QA Validation Specialist, CSV & Equipment role is an exempt level position with responsibilities for providing quality oversight over the validation and qualification activities for equipment, systems, computer systems, and processes within a cell therapy manufacturing plant to support both clinical and commercial requirements in a sterile GMP environment. ...

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  • 11 days ago

    MES Project Manager

    Legend Biotech USA - Raritan, NJ, United States

    Legend Biotech is seeking MES Project Manager as part of the Manufacturing Excellence team based in Raritan, NJ.Role OverviewThe MES Project Manager will be part of Manufacturing Science and Technology team reporting to the Manufacturing Execution Systems Lead and will be responsible for providing project management support to the development and administration of EBR and digital solutions at the Raritan site to support base business production processing while liaising with other functions ...

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  • 11 days ago

    Equipment Automation Intern

    Legend Biotech USA - Raritan, NJ, United States

    Legend Biotech is seeking an Equipment Automation Intern as part of the Facilities & Engineering team based in Raritan, NJ. Role OverviewThe Equipment Automation Intern will support the Instrument Automation team in managing and maintaining computerized systems within a GMP manufacturing environment. This role involves assisting with compliance activities, troubleshooting equipment connectivity, and supporting documentation and data integrity efforts. The intern will gain exposure to regulatory ...

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  • 12 days ago

    QA Investigations Lead II

    Legend Biotech USA - Raritan, NJ, United States

    Legend Biotech is seeking QA Investigations Lead I as part of the Quality team based in Raritan, NJ. Role OverviewThe QA Investigation Lead is an exempt level position reporting to the QA Investigation Supervisor within the Raritan Investigation Excellence Team. The QA Investigations Lead is responsible for providing quality oversight and guidance during the investigation of events that occur in the production of a personalized cell therapy product in a sterile GMP environment. The ideal candidate ...

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  • 13 days ago

    QA Validation Specialist I/II/III

    Legend Biotech USA - Raritan, NJ, United States

    Legend Biotech is seeking a QA Validation Specialist II/IIIas part of the Quality team based in Raritan, NJ.Role Overview The QA Validation Specialist role is an exempt level position with responsibilities for providing quality oversight over the validation and qualification activities for equipment, systems, computer systems, and processes within a cell therapy manufacturing plant to support both clinical and commercial requirements in a sterile GMP environment. This role will also provide ...

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  • 13 days ago

    QA Change Control Specialist II

    Legend Biotech USA - Raritan, NJ, United States

    Legend Biotech is seeking a QA Change Control Specialist II as part of the Quality team based in Raritan, NJ.Role OverviewThe QA Change Control Specialist II role is an exempt level position with responsibilities for providing quality oversight over the change control process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment. This role will be responsible for managing change control activities throughout the lifecycle. ...

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