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Legend Biotech

Develops and commercializes cell therapies

QA Warehouse Specialist 3

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeRaritan, NJ, USA

About the Job

Requirements

  • Zero to four years of relevant work experience is required.
  • Proficiency in quality systems such as SAP is required.
  • Knowledge of current Good Manufacturing Practice regulations and Food and Drug Administration and European Union guidance related to manufacturing cell-based products is required.
  • Knowledge of Good Tissue Practice is required.
  • Candidates must be able to accommodate unplanned overtime, including nights and weekends, on little to no prior notice.

Responsibilities

  • Support warehouse activities related to material receipt, handling, and release, as well as incoming and release of patient material and final product at the Raritan CAR-T manufacturing site.
  • Participate in the quality team responsible for incoming inspection and release of materials used in manufacturing autologous CAR-T products for clinical trials and commercial operations in a controlled current Good Manufacturing Practice environment.
  • Review, inspect, and disposition incoming materials for use in CAR-T product manufacturing according to the inspection plan, and record results to complete the receipt process.
  • Review inspection documentation, such as Certificates of Analysis or other material certifications, for inbound materials.
  • Conduct routine housekeeping checks of the warehouse and supporting areas.
  • Routinely review warehouse documents and logbooks to ensure adherence to Good Documentation Practices.
  • Ensure that all materials are in the proper location and under the appropriate storage conditions.
  • Make appropriate quality decisions in support of warehouse activities.
  • Ensure cycle counts are accurate and performed in a timely manner according to procedures.
  • Review and inspect documentation supporting final product shipments.
  • Generate inspection reports and non-conformances for failures as required.
  • Scan, file, and archive quality assurance-related documents.
  • Update the supervisor on work status or problems, with recommendations for improvement or correction.
  • Investigate non-conformances thoroughly, approve them in a timely manner, and ensure appropriate corrective and preventive action plans are implemented.
  • Reduce non-conformances in supported areas by driving compliance.
  • Perform tasks consistently with safety policies, quality systems, and current Good Manufacturing Practice requirements.
  • Perform other duties as assigned.

Desired Qualifications

  • Experience working in a current Good Manufacturing Practice manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, or cell therapy.
  • Experience in clinical quality, method development, cell banking, or research and development.
  • Experience working with cell therapy.

About the Company

Legend Biotech

Develops and commercializes cell therapies

Legend Biotech develops and commercializes cell therapies for serious diseases, especially hematological cancers and solid tumors, using multiple technology platforms. Its CAR-T therapies modify a patient’s own T cells to fight cancer, and the company licenses and sells these therapies while pursuing additional research. By pursuing a technology-agnostic pipeline, Legend Biotech aims to bring effective, personalized treatments to patients globally. The company also maintains investor communications to share progress and results.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Bridgewater Township, New Jersey
Founded
2014

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