Drimva

Legend Biotech

QA Warehouse Specialist III

$96K–$126K

Raritan, New Jersey, United States · Full-time · Posted Oct 20, 2026

Experience
0-4 years of relevant work experience required.
Visa sponsorship
Applicants must be authorized to work in the United States; employment eligibility is verified through E-Verify.

About the job

Supports quality assurance for warehouse material receipt, inspection, storage, release, and final-product shipments at a CAR-T manufacturing site.

What you'll do

  • Inspect and disposition incoming manufacturing materials, reviewing certifications and recording receipt results.
  • Check warehouse conditions, storage, records, and cycle counts for compliance with procedures and quality requirements.
  • Review final-product shipment documentation and support investigation and corrective actions for non-conformances.

What they ask for

  • Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing cell-based products.
  • Knowledge of Good Tissue Practice.
  • Proficiency with quality systems such as SAP.
  • Excellent written and oral communication skills; must accommodate unplanned overtime, including nights and weekends, on little to no prior notice.

Nice to have

  • Experience in a cGMP manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, or cell therapy.
  • Experience in clinical quality, method development, cell banking, Research & Development, or cell therapy.

Pay

$96,267 — $126,351 USD (base salary)

Tools

SAP, CAR-T, cGMP, FDA/EU

Model-written summary · the original posting is authoritative

First seen Oct 29, 2026 · Last verified Nov 5, 2026 (UTC)