Associate Cell Therapy Manufacturing

About the Role:

We are seeking a highly motivated Associate to join a Manufacturing team supporting cell-based cancer immunotherapy production. This role supports tech transfer and operational readiness, applying cGMP knowledge to ensure manufacturing readiness. Core responsibilities include ensuring the successful, time-sensitive GMP manufacture and release of cell therapy products, following all cGMP/CFR/site quality system requirements, and promoting a culture of quality and compliance.

Location: South San Francisco, CA | Type: 6-month contract with potential extension | Compensation: $40-$44/hr | Hours: M-F 1st Shift

The ideal candidate has experience in a regulated biotech or pharmaceutical setting with proven competency in GMP manufacture of cell-based therapies.

Responsibilities:
• Perform process unit and support operations per SOPs and batch records, including PBMC/media/solution preparation, cell drug substance preparation, and drug product fill operations
• Complete required documentation accurately and on time per protocols, SOPs, and batch records
• Maintain aseptic technique throughout processing to preserve product integrity, viability, and sterility from cell thaw through final formulated drug product cryopreservation
• Perform tasks consistent with safety policies, quality systems, and cGMP requirements
• Complete training assignments on time to maintain compliant technical skills and knowledge
• Assist in setting up manufacturing areas and equipment, including automated cell processing, expansion, and filling equipment
• Update and revise manufacturing operating procedures for technical soundness, efficiency, and cGMP compliance
• Monitor, clean, prepare, and operate processing and analytical equipment in Grade B/C areas

Requirements:
• Bachelor's or Associate's degree in a relevant science or engineering discipline
• 0-2 years of experience in cGMP biologics or cell therapy manufacturing
• Aseptic processing experience in Grade A biosafety cabinets and Grade B clean rooms
• Cell culture processing experience with human primary cells strongly preferred
• Familiarity with universal precautions for handling human-derived materials in BSL-2 containment
• Knowledge of cGMP regulations and FDA guidance for biologics and/or cell therapy
• Excellent interpersonal, oral, and written communication skills
• Ability to work off-shift and long hours as required
• Physical requirements: frequent lifting/carrying/pushing/pulling up to 30 lbs, frequent sitting/walking/standing, frequent PPE use, occasional climbing/bending/stooping/crouching, occasional fine finger dexterity, occasional use of hazardous materials/chemicals, occasional work in cold rooms/freezers, color/vision/depth perception required
• Must be authorized to work in the U.S.

This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!