legendcareers

Operations Supervisor

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At a Glance

Location
Raritan, New Jersey, United States
Work Regime
onsite
Experience
6+ years
Posted
2026-06-22T16:13:32-04:00

Key Requirements

Required Skills

ExcelMicrosoft OfficePowerPoint

Certifications

  • Lean

Domain Knowledge

  • Biotech
  • Engineering
  • Insurance
  • Legal
  • Manufacturing
  • Medical

Requirements

A minimum of 6 years of operations experience within a cGMP environment in the biotech/biopharma industry.

Prior experience in manufacturing, quality, or engineering is required.

Knowledge of cGMP regulations and FDA guidance related to manufacturing of cell-based products, and cleanroom behaviors.

An ability to build strong partnerships and effectively integrate with external collaborators to drive projects/programs forward in a matrixed environment.

Experience with Operational Excellence and/or Lean Manufacturing is an asset.

Compensation & Benefits

$96,267

$126,351 USD

Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.

Responsibilities

The CAR-T Operations Supervisor is an exempt level position working within Technical Operations team, responsible for directing the daily production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment.

This individual will lead and supervise multiple units within the CAR-T process operations (i.e.

component preparation manufacturing, MFG support operations, Mock cell, and CAR-T process) according to standard operating procedures and batch records and ensure safe and compliant manufacturing operations according to cGMP requirements.

This individual’s primary responsibility will be to work closely with operations personnel on the production floor to provide guidance and perform production tasks as needed to help the team, in a manner consistent with safety policies, quality systems, and cGMP requirements.

This individual will support manufacturing investigations, create/revise operational procedures, including manufacturing work instructions, master batch records, forms, and support and manage change controls.

This individual will work closely with Operations Manager to help oversee the development of production personnel, provide input on personnel performance.

About the Company

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