Cell Therapy Process Development Lab Technician (cGMP)

University of Southern California; Glendale (CA); On-site; USD 36,000 - 41,000; Full time

Job summary

The University of Southern California invites applications for a Process Development (PD) Specialized Lab Technician at the USC/CHLA cGMP Facility in Los Angeles. The role supports scale-up and optimization of cell therapy processes, conducts experiments, prepares equipment, and collects data to advance development studies.

Candidates should hold a Bachelor's in Biological Sciences or Biotechnology, have 2+ years in cell therapy development, and be familiar with FDA regulations.

Qualifications

• Degree in a directly related specialized scientific field.
• Demonstrated knowledge of biotechnology and cell therapy.
• Experience with FDA regulations and clinical trials.
• Strong communication and writing skills; ability to work independently and in a team.

Responsibilities

• Performs moderate to complex laboratory procedures related to cell therapy development and quality control testing in a cGMP environment.
• Maintains and calibrates lab equipment; ensures clean, safe, and organized work areas.
• Monitors inventory and coordinates supplies for ongoing operations.
• Collects and documents data; supports technology transfer from development to manufacturing.
• Stays current with regulations and best practices in cell therapy and cGMP manufacturing.

Skills

Communication skills

Team collaboration

Attention to detail

SOP compliance

cGMP experience

Regulatory knowledge

Education

Bachelor's degree in Biological Science and/or Biotechnology

Job description

The University of Southern California invites applications for a Process Development (PD) Specialized Lab Technician at the USC/CHLA cGMP Facility in Los Angeles. The role supports scale-up and optimization of cell therapy processes, conducts experiments, prepares equipment, and collects data to advance development studies.

Candidates should hold a Bachelor's in Biological Sciences or Biotechnology, have 2+ years in cell therapy development, and be familiar with FDA regulations.