Legend Biotech is seeking Quality Compliance Lead as part of the Quality team based in Raritan, NJ.
Role Overview
The Quality Compliance- Lead Auditor CAR-T is responsible for regulatory compliance supporting the production of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom environment.
Key Responsibilities
- Successfully support the implementation, execution, and improvement of the internal audit process.
- Support the planning and execution of internal audits for all quality system areas for the manufacturing site; write audit reports, issue audit observations and follow-through to ensure satisfactory resolution and closure of each internal audit.
- Coordinate front room/ back room activities for health authority audits and independent audits; manage audit responses and observation resolution.
- Drive site compliance to regulatory, enterprise, and global requirements through building positive relationships across functions, to meet unified business objectives.
- As required, run reports and conduct data analysis to support monitoring of key performance indicators; support the preparation of compliance data for the monthly CRB & quarterly QSMR presentations.
- Fulfills the Quality System audit module site key user responsibilities - represent the Raritan site in global forums/ team meetings, mentor site users for audit process, and control access to any systems used to support audits/inspections.
- Provide support to quality systems team, ad hoc, for activities such as annual product review, site risk register, or internal quality agreements.
- Develops and delivers training for specific quality system topics, in both classroom setting and individual interactions
- Support the creation, assessment and closure as needed of corrective actions, change controls, or audit actions related to the site
- Ensures and maintains a state of inspection readiness.
- Perform compliance walkthroughs as part of audit/inspection readiness activities to ensure that the site is an inspection ready state.
- Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.
- A minimum of a Bachelor’s Degree in Engineering, Science or equivalent technical discipline is required
- A minimum of five (5) years of experience in Quality Assurance/ Quality Systems or Compliance
- Experience conducting internal audits (self-inspection), including writing audit reports, writing observations, and follow-through of observation resolution
- Experience in front room/ back room roles for external audits
- Experience working with quality systems is required
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Legend Biotech is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is Legend’s policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
Legend Biotech maintains a drug-free workplace.
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What We Do
Legend Biotech is a global, commercial-stage biotechnology company developing and manufacturing novel therapies. We explore and apply innovative technologies to deliver cutting-edge options for patients around the world.
Our corporate headquarters is located in Somerset, NJ, and our manufacturing footprint includes facilities in the United States, China and the Belgium.
