Drimva

Legend Biotech

Operations Support Specialist

$48K–$63K

Raritan, New Jersey, United States · Full-time · Posted Aug 21, 2026

Experience
A minimum of 0-1 years of operations experience in a cGMP environment in the biotech/biopharma industry.
Education
Bachelor’s degree in engineering or related field or equivalent experience required.
Visa sponsorship
Applicants must be authorized to work in the United States; the company participates in E-Verify.

About the job

Performs cell therapy manufacturing operations in a sterile cGMP environment to support clinical and commercial production.

What you'll do

  • Carry out cell culture, purification, aseptic processing, and cryopreservation according to SOPs and batch records, documenting production data.
  • Follow safety, quality, and cGMP requirements and coordinate with Manufacturing, Engineering, and Quality to complete shift production tasks.
  • Support manufacturing process development and continuous improvement.

What they ask for

  • Bachelor’s degree in engineering or related field, or equivalent experience.
  • Knowledge of cGMP regulations and FDA guidance related to manufacturing cell-based products.
  • Ability to handle human-derived materials in a BSL-2 cleanroom facility and lift at least 50 lbs.
  • Ability to accommodate shift work, including evenings and weekends, and unplanned overtime.

Pay

$47,861 — $62,819 USD (base salary)

Tools

cGMP, FDA

Model-written summary · the original posting is authoritative

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