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$34

How much do cell therapy manufacturing jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for cell therapy manufacturing in the United States is $24.95, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $28.85 per hour, depending on experience, location, and employer.

What are some common challenges faced in cell therapy manufacturing, and how can new team members prepare for them?

Cell Therapy Manufacturing professionals often encounter challenges such as maintaining strict aseptic conditions, managing complex documentation requirements, and ensuring compliance with evolving regulatory standards. New team members can prepare by familiarizing themselves with Good Manufacturing Practices (GMP), developing strong attention to detail, and staying current on industry regulations. Collaboration with quality control, process development, and regulatory teams is essential for troubleshooting and continuous improvement in this rapidly advancing field.

What is cell therapy manufacturing?

Cell therapy manufacturing is the process of producing living cells that can be used as therapeutic treatments for diseases, such as cancer or genetic disorders. This involves growing, modifying, and preparing cells in a controlled environment to ensure they are safe and effective for patient use. The process must meet strict regulatory standards to ensure product quality, consistency, and patient safety. Cell therapy manufacturing is a vital part of the biotechnology and pharmaceutical industries, supporting advanced treatments like CAR-T cell therapy and stem cell transplants.

What does a cell therapy manufacturing associate do?

A cell therapy manufacturing associate is responsible for preparing, processing, and assembling cell-based products in a laboratory or manufacturing setting. They follow strict protocols, operate specialized equipment, and ensure quality control to produce safe and effective therapies, often working in cleanroom environments and adhering to Good Manufacturing Practices (GMP).

What are the key skills and qualifications needed to thrive in cell therapy manufacturing?

To excel in Cell Therapy Manufacturing, a strong background in biology or biotechnology, laboratory techniques, and GMP (Good Manufacturing Practice) compliance is essential, often supported by a relevant degree or certification. Familiarity with bioprocessing equipment, aseptic techniques, and electronic batch record systems is typically required. Attention to detail, teamwork, and strong problem-solving skills help individuals adapt to the complex and regulated environment. These competencies ensure the safe, reliable, and high-quality production of cell-based therapies critical for patient treatment.

What is the difference between Cell Therapy Manufacturing vs Cell Culture Technician?

AspectCell Therapy ManufacturingCell Culture Technician
Required CredentialsTypically requires a Bachelor's degree in biology, biotechnology, or related field; certifications in GMP or cell processing are commonUsually requires a high school diploma or associate degree; some roles may need basic lab certifications
Work EnvironmentCleanroom, GMP-compliant manufacturing facilities, regulated environmentLaboratories, research facilities, or production areas, often less regulated
Employer & Industry UsageBiotech, pharmaceutical companies, cell therapy manufacturing plantsResearch labs, biotech companies, academic institutions

Cell Therapy Manufacturing involves working in regulated, GMP-compliant environments to produce cell-based therapies, requiring specialized training and certifications. In contrast, Cell Culture Technicians focus on maintaining cell cultures in research or less regulated settings, with generally fewer certifications needed. Both roles are essential in the biotech industry but differ in scope, environment, and credential requirements.

More about Cell Therapy Manufacturing jobs
What cities are hiring for Cell Therapy Manufacturing jobs? Cities with the most Cell Therapy Manufacturing job openings:
What states have the most Cell Therapy Manufacturing jobs? States with the most job openings for Cell Therapy Manufacturing jobs include:
What job categories do people searching Cell Therapy Manufacturing jobs look for? The top searched job categories for Cell Therapy Manufacturing jobs are:
Cell Therapy Manufacturing jobs near you
Infographic showing various Cell Therapy Manufacturing job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 71% Full Time, 27% Part Time, and 1% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $51,890 per year, or $24.9 per hour.

Cell Therapy Manufacturing Specialist

Kelly Services

South San Francisco, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 12 days ago

Job description

Cell Therapy Manufacturing Associate
Multiple Positions
Location: South San Francisco, CA 94080
Company: Cell Therapy Manufacturing
Target Salary: $35-$40; BOE
Available Shifts
Day Shift
  • 7:00 AM – 7:30 PM | Sunday – Tuesday, alternating Wednesdays
  • 7:00 AM – 7:30 PM | Thursday – Saturday, alternating Wednesdays
Night Shift
  • 7:00 PM – 7:30 AM | Sunday – Tuesday, alternating Wednesdays
  • 7:00 PM – 7:30 AM | Thursday – Saturday, alternating Wednesdays
Initial Training Schedule
  • Monday – Friday, 9:00 AM – 5:30 PM
Position Summary
Seeking a highly motivated Cell Therapy Manufacturing Associate to support the development and production of advanced cell therapy products. This role will contribute to both GMP manufacturing operations and laboratory activities within a fast-paced, collaborative environment focused on advancing innovative therapies.
The ideal candidate is detail-oriented, committed to quality and compliance, and passionate about supporting cutting-edge biotechnology and cell therapy manufacturing.
Key Responsibilities
  • Execute manufacturing processes in both R&D and GMP environments following approved procedures, batch records, protocols, and SOPs.
  • Perform routine laboratory and manufacturing activities, including reagent preparation, leukopak processing, and sample testing.
  • Operate within a controlled GMP environment and perform cleanroom gowning according to established procedures.
  • Support process development efforts by providing operational feedback to engineering and process science teams.
  • Assist with process, equipment, and cleaning validation activities.
  • Contribute to the analysis, documentation, and presentation of technical results.
  • Perform routine laboratory and cleanroom maintenance, including cleaning, stocking, ordering supplies, and equipment qualification/maintenance.
  • Complete all required training and maintain compliance with internal policies, GMP requirements, and safety standards.
  • Prepare, review, revise, and maintain manufacturing documentation, including batch records, SOPs, protocols, and reports.
  • Initiate, investigate, and support the closure of deviations, CAPAs, and related quality documentation.
  • Review manufacturing records for accuracy and ensure timely submission of completed documentation.
  • Train and mentor new team members on manufacturing procedures, aseptic techniques, equipment operation, and troubleshooting.
  • Collaborate cross-functionally with Quality Assurance, Quality Control, Validation, Facilities, Materials Management, and other departments to support manufacturing objectives.
  • Perform additional duties as assigned.
Qualifications
Required
  • Bachelor’s degree, associate degree, technical diploma, or equivalent education in a scientific or related field.
  • Minimum 1 year of experience in biotechnology, biopharmaceutical manufacturing, or a related GMP-regulated environment.
  • Experience following SOPs, batch records, protocols, and GMP documentation requirements.
  • Strong attention to detail and commitment to quality, compliance, and safety.
  • Excellent communication, organizational, and interpersonal skills.
  • Strong analytical and problem-solving abilities.
Preferred
  • Experience in cell and gene therapy manufacturing.
  • Experience working in cGMP operations and cleanroom environments.
  • Familiarity with drug product manufacturing equipment and aseptic processing techniques.
Why Join our team?
You have the opportunity to work alongside talented scientists and manufacturing professionals developing transformative cell therapy technologies. We offer a collaborative environment where innovation, quality, and patient impact drive everything we do.
#P1
 
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
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