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Cell Therapy Manufacturing Associate

Job in Los Angeles, Los Angeles County, California, 90079, USA
Listing for: Infotree Global Solutions
Full Time position
Listed on 2026-03-06
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Validation Engineer, Operations Engineer, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Schedule

Schedule: Monday–Friday, 8 hours/day (may transition to 4x10 shift: Sun–Wed or Wed–Sat)

Key Responsibilities
  • Execute manufacturing activities in accordance with established batch records, SOPs, and cGMP regulations
  • Operate and maintain automated and semi-automated cell therapy processing equipment
  • Perform aseptic processing in ISO 5 cleanroom environments
  • Support facility and equipment readiness, including installation, qualification, and maintenance coordination
  • Assist with technology transfer activities for new or pipeline products
  • Participate in deviation investigations and documentation support
  • Prepare, stage, and verify materials and components required for manufacturing
  • Ensure accurate and timely completion of manufacturing documentation
  • Maintain cleanroom inventory levels and coordinate material replenishment
  • Collaborate cross-functionally with Process Development and MSAT teams
  • Provide updates to leadership regarding production status and operational needs
Required Equipment Experience
  • NC-200 Nucleocounter Automated Cell Counter
  • Cue
  • Sealer
  • Microscope
  • Sefia
  • Sepax

Experience in CAR‑T immunotherapy production as an operator, verifier, or runner is strongly preferred.

Qualifications
  • High School Diploma with minimum 5 years of relevant GMP manufacturing experience
  • OR
  • Bachelor’s degree in a scientific or engineering discipline with relevant hands‑on manufacturing experience
  • Strong understanding of cGMP regulations and biologics manufacturing practices
  • Knowledge of CMC regulatory requirements
  • Experience with primary human cell culture and aseptic technique
  • Familiarity with deviation management and GMP documentation systems
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Position Requirements
10+ Years work experience
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