QC, Investigations Specialist II​/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.

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 QC, Investigations Specialist II/III as part of the Quality team based in Raritan, NJ
.

The QC Investigations Specialist is an exempt level position with responsibilities for leading deviations and corrective actions in support of the QC testing laboratories related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment.

Mon‑Fri, 1st Shift

• Interview personnel within QC and provide quality insight to complete laboratory investigation reports in Trackwise.
• Review/complete routine CAR‑T manufacturing nonconformance/deviation investigations.
• Proactively work with stakeholders to implement effective CAPAs and to ensure the timely completion of corrective and preventive actions within the laboratories.
• Provide recommendations for the improvement of processes by working cross‑functionally with multiple stakeholders.
• Work closely with management to propose/execute improvements through the change management system.
• Respond with a high degree of urgency to departmental and cross‑functional needs and requests.
• Reporting/monitoring metrics on non‑conformance investigations and corrective and preventive actions (CAPA).
• Perform tasks in a manner consistent with the safety policies, quality systems and cGM Prequirements.
• Work in a collaborative team setting with quality counterparts that include Quality Assurance, Manufacturing Operations, and Analytical/Process Development.

• A minimum of a Bachelor’s Degree in Science, Engineering or equivalent technical discipline is required.
• A Minimum of 4 years relevant work experience, preferably within a biological and/or pharmaceutical industry is required.
• Experience in a Quality Control setting is preferred.
• Experience with aseptic processing in ISO 5 clean room and biosafety cabinets is required.
• Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell‑based products is required.
• Knowledge of Good Tissue Practices is required.
• Detailed knowledge of CAR‑T QC test methods and related equipment is preferred.
• Excellent written and oral communication skill are required.
• Candidates must be able to accommodate shift schedule. Shifts include routine weekend and evening work as required by the manufacturing process.
• Candidates must be able to accommodate unplanned overtime (including nights and weekends) on little to no prior notice.
• The candidate must be highly organized and capable of working in a team environment with a positive attitude under some supervision.
• Comfortable with speaking and interacting with inspectors.
• This position may require occasional travel to partner sites in NJ or PA as business demands.
• This position may require up to 10% domestic or international travel as business demands.

$75,972 - $99,713 USD

We are committed to creating a workplace where employees can thrive - both professionally and personally. To attract and retain top talent in a highly competitive industry, we offer a best‑in‑class benefits package that supports well‑being, financial stability, and long‑term career growth. Highlights include medical, dental, and vision insurance as well as a 401(k)‑retirement plan with company match that vest fully on day one.

Equity and stock options are available to employees in eligible roles. We offer eight weeks of paid…