Operations Associate

Legend Biotech, Inc.; Raritan (NJ); On-site; USD 65,000 - 90,000; Full time

Job summary

Legend Biotech, Inc. is seeking a Manufacturing Operations Associate to support autologous CAR-T production in a cGMP environment. You will execute manufacturing steps and maintain strict documentation to ensure quality and compliance.

Based in Raritan, NJ, this on-site role emphasizes safety, process development support, and continuous improvement within Legend Biotech's manufacturing team.

Qualifications

• HS diploma with 3-5 years biotech/pharmaceutical experience, or associate degree with 2-3 years, or bachelor’s degree with up to 2 years industry experience.
• Knowledge of cell therapy manufacturing, GMP compliance, and equipment operation.
• Ability to work in a controlled environment and lift up to 25 lbs.

Responsibilities

• execute manufacturing processes for cell therapies, including cell culturing, purification, aseptic processing, and cryopreservation
• maintain documentation and comply with quality standards
• support process development and continuous improvement
• ensure safety and adherence to GMP regulations

Skills

Cell therapy

GMP compliance

Equipment operation

Biotech/pharma experience

Education

HS diploma

Associates degree

Bachelor's degree

Tools

Process excellence tools

Laboratory techniques

Biological material handling

Job description

Role

Manufacturing Operations Associate supporting autologous CAR-T production in a cGMP environment within Legend Biotech's manufacturing team.

Responsibilities

• execute manufacturing processes for cell therapies, including cell culturing, purification, aseptic processing, and cryopreservation
• maintain documentation and comply with quality standards
• support process development and continuous improvement
• ensure safety and adherence to GMP regulations

Requirements

• HS diploma with 3-5 years biotech/pharmaceutical experience, or associate’s degree with 2-3 years, or bachelor’s degree with up to 2 years industry experience
• knowledge of cell therapy manufacturing, GMP compliance, and equipment operation
• ability to work in a controlled environment and lift up to 25 lbs.

Preferred

• familiarity with process excellence tools, laboratory techniques, and biological material handling

High-value specifics

focus on autologous CAR-T manufacturing, in a controlled clinical and commercial setting, contributing to innovative cell therapy development.

Work setup

based in Raritan, NJ, with routine on-site work and compliance with safety protocols.