Cell Therapy Manufacturing Associate (Day &Night)

By | June 23, 2026

Cell Therapy Manufacturing Associate (Day &Night)

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Job ID: 10276943

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South San Francisco, CA, US

Scientific

Bachelors Degree

Full Time, Temporary

$35.00-40.00/hour

Experienced (Non-Manager)

On-site

Biotechnology/Pharmaceuticals

First Shift (Day)

South San Francisco, CA, US

$35.00-40.00/hour

Experienced (Non-Manager)

Full Time, Temporary

Biotechnology/Pharmaceuticals

On-site

Scientific

Bachelors Degree

First Shift (Day)

Apply Now Applied

Job details

Kelly Science & Clinical is seeking a Cell Therapy Manufacturing Associate for a 6 month project with an exciting company located in South San Francisco, CA.
 
Position Summary:
Join a dynamic Process Sciences team as a Cell Therapy Manufacturing Associate! You will help develop and manufacture advanced cell therapy products in a fast-paced, mission-driven environment.
 
Shift Available:

  • Day Shifts:

    • Sunday–Tuesday; alternating Wednesday (7:00 AM – 7:30 PM)

    • Thursday–Saturday; alternating Wednesday (7:00 AM – 7:30 PM)


  • Night Shifts:

    • Sunday–Tuesday; alternating Wednesday (7:00 PM – 7:30 AM)

    • Thursday–Saturday; alternating Wednesday (7:00 PM – 7:30 AM)

 
Employment Type: 6 month contract
 
Pay:

  • Day Shift: $35.00-38.50/hour

  • Night Shift: $38.50-40.00/hour

 
Key Responsibilities:

  • Execute routine manufacturing and laboratory operations, adhering to SOPs and protocols in both R&D and cGMP environments.

  • Prepare reagents, process leukopaks, and support sample testing.

  • Provide technical feedback and collaborate with engineering and process teams.

  • Support equipment qualification, validation, cleaning, ordering, and restocking.

  • Maintain compliance with internal and external control procedures, completing required training.

  • Author, revise, and review production records and SOPs for accuracy.

  • Assist in deviations, CAPA closures, and mentor new associates.

  • Collaborate with Quality, Facilities, Materials Management, and Validation teams.

  • Other duties as needed.

Requirements:

  • Bachelor’s degree or diploma in a scientific or related field.

  • 1+ year experience in biotech/biopharma cGMP operations, preferably cell and gene therapy.

  • Experience following protocols, SOPs, GMP documentation.

  • Proficiency in operating process equipment for drug product manufacturing.

  • Committed to job safety and compliance.

  • Excellent communication and problem-solving skills.

  • Self-motivated, growth-minded, and passionate about advancing cell therapy.

 
Ready to make an impact? Apply today to help shape the future of cell therapy!
 

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