Senior QA Warehouse Specialist – cGMP Materials CAR‑T

Legend Biotech US; Raritan (NJ); On-site; USD 96,000 - 126,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

401(k) plan with company match

Paid parental leave

Paid time off

Job summary

Legend Biotech US is hiring a QA Warehouse Specialist III for our Raritan, NJ site. You will support receipt, handling and release of materials and patient-related final product, ensuring adherence to cGMP and GDP standards.

The role involves reviewing documentation, performing inspections, and maintaining accurate warehouse records. The ideal candidate has up to four years in a cGMP environment, experience with SAP, and strong communication skills to support regulatory compliance and quality

Qualifications

• 0–4 years of relevant work experience in a cGMP manufacturing facility.
• Experience in clinical quality, method development, or cell therapy is preferred.
• Proficiency with quality systems such as SAP and familiarity with GDP/cGMP standards.

Responsibilities

• Support Warehouse activities related to material receipt, handling and release.
• Inspect, disposition and record results for inbound materials per plan.
• Review documentation for inbound materials and final product shipments.
• Maintain accurate cycle counts and ensure proper storage conditions.

Skills

Quality systems

SAP

Excellent communication

cGMP knowledge

Education

No specific degree stated

Tools

SAP

Job description

Legend Biotech US is hiring a QA Warehouse Specialist III for our Raritan, NJ site. You will support receipt, handling and release of materials and patient-related final product, ensuring adherence to cGMP and GDP standards.

The role involves reviewing documentation, performing inspections, and maintaining accurate warehouse records. The ideal candidate has up to four years in a cGMP environment, experience with SAP, and strong communication skills to support regulatory compliance and quality