Drimva

Legend Biotech

Operations Supervisor

$96K–$126K

Raritan, New Jersey, United States · Full-time · Posted Jun 22, 2026

Experience
A minimum of 6 years of operations experience within a cGMP environment in the biotech/biopharma industry.
Education
Bachelor’s degree in Science, 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

Supervises daily CAR-T cell therapy production on an assigned shift in a sterile cGMP environment, ensuring safe, compliant manufacturing and supporting clinical and commercial production.

What you'll do

  • Lead shift meetings, assign production tasks, supervise operations, and assist with production work as needed.
  • Support manufacturing investigations, procedures, batch records, forms, and change controls.
  • Partner with Manufacturing, Engineering, and Quality to resolve production issues and improve processes.

What they ask for

  • Bachelor’s degree in Science, Engineering or related field or equivalent experience.
  • Minimum 6 years of operations experience within a cGMP environment in biotech/biopharma; prior manufacturing, quality, or engineering experience required.
  • Knowledge of cGMP regulations, FDA guidance related to cell-based product manufacturing, and cleanroom behaviors.
  • Proficiency with Microsoft Office tools (Word, Excel, PowerPoint, and Outlook); availability for shift work, including evenings and weekends as required.

Nice to have

  • Experience with Operational Excellence and/or Lean Manufacturing.

Pay

$96,267 — $126,351 USD (base salary)

Tools

Microsoft Office, Word, Excel, PowerPoint, Outlook

Model-written summary · the original posting is authoritative

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