Biotech Manufacturing Operator — CAR-T & Cell Therapy

Legend Biotech EU

Raritan (NJ)

On-site

USD 59,000 - 78,000

Full time

11 days ago

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Benefits offered by this job

Medical, dental, and vision insurance
401(k) with company match
Paid parental leave
Paid time off with holidays

Job summary

Legend Biotech USA Inc. is seeking an Operations Associate for the Manufacturing & Supply team in Raritan, NJ.

The role focuses on executing CGMP manufacturing procedures, including autologous CAR‑T product production, while maintaining high quality and compliance standards. You will work in a cross-functional team to perform cell culture, purification, aseptic processing, and documentation, supporting continuous improvement and on-time production.

Qualifications

  • HS Diploma required with 3–5 years Biotech/Pharmaceutical experience or equivalent industry experience.
  • Associates Degree in Life Sciences or Manufacturing with 2–3 years related experience.
  • Bachelor's Degree in Life Sciences with 0–2 years Biotech/Pharmaceutical experience or equivalent industry experience.

Responsibilities

  • Perform manufacturing procedures and scheduled tasks within a CGMP environment.
  • Execute manufacturing processes including cell culture, purification, aseptic processing and cryopreservation.
  • Record production data accurately in GMP documentation and batch records.
  • Work in a team-based, cross-functional environment to meet shift production goals.
  • Support process development and drive continuous improvements in manufacturing operations.
  • Handle human-derived materials in containment areas and ensure safety and compliance.

Job description

Legend Biotech USA Inc. is seeking an Operations Associate for the Manufacturing & Supply team in Raritan, NJ.

The role focuses on executing CGMP manufacturing procedures, including autologous CAR‑T product production, while maintaining high quality and compliance standards. You will work in a cross-functional team to perform cell culture, purification, aseptic processing, and documentation, supporting continuous improvement and on-time production.

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