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Cell Therapy Technologist Jobs (NOW HIRING)

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Cellular Therapy Technologist

Las Vegas, NV · On-site

Knowledge and experience of hematopoietic stem cell / CAR-T cell processing and protocols ... Cellular Therapy Technologist opening. We promptly review all applications. Highly qualified ...

New

AstraZeneca

Lead Cell Therapy Specialist

Tarzana, CA · On-site

$81K - $122K/yr

Experience supporting technology transfer and GMP clinical or commercial manufacturing operations ... cell therapy manufacturing? Apply today and help lead the execution, quality, and teamwork that ...

AstraZeneca

Lead Cell Therapy Specialist

Los Angeles, CA · On-site

$81K - $122K/yr

Experience supporting technology transfer and GMP clinical or commercial manufacturing operations ... cell therapy manufacturing? Apply today and help lead the execution, quality, and teamwork that ...

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Cell Therapy Technologist information

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How much do cell therapy technologist jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for cell therapy technologist in the United States is $17.41, according to ZipRecruiter salary data. Most workers in this role earn between $14.90 and $19.23 per hour, depending on experience, location, and employer.

What is a cell therapy technologist?

Cell Therapy Technologists are specialized laboratory professionals who process, prepare, and test cellular products used in advanced medical treatments, such as stem cell transplants and immunotherapies. They work in hospitals, research labs, and biomanufacturing facilities, ensuring that cell-based therapies are safe, effective, and meet regulatory standards. Their responsibilities include handling cell cultures, performing quality control tests, and maintaining accurate records. This role is vital for supporting cutting-edge treatments in oncology, regenerative medicine, and other fields.

What challenges do cell therapy technologists face during the manufacturing process, and how are they addressed?

Cell Therapy Technologists often encounter challenges such as maintaining strict aseptic conditions, ensuring product consistency, and adhering to rigorous regulatory standards. Variability in donor material and the complexity of cell manipulation can make reproducibility difficult. To address these challenges, technologists follow standardized protocols, perform thorough documentation, and work closely with quality assurance teams. Continuous training and collaboration with cross-functional teams—such as research scientists and clinical staff—are also key to overcoming these hurdles and ensuring patient safety.

What is the difference between Cell Therapy Technologist vs Laboratory Technician?

AspectCell Therapy TechnologistLaboratory Technician
CredentialsTypically requires a bachelor's degree in biology, biotechnology, or related field; certifications in cell processing may be preferredUsually requires an associate degree or diploma in laboratory sciences or related field
Work EnvironmentSpecialized cell processing labs, hospitals, or biotech companies focusing on cell therapiesGeneral laboratory settings across various industries including research, clinical, or industrial labs
Industry UsagePrimarily in biotech, pharmaceutical, and healthcare sectors involved in cell therapy development and manufacturingBroadly used across research, clinical diagnostics, and industrial manufacturing

The main difference between a Cell Therapy Technologist and a Laboratory Technician lies in their specialization and work environment. Cell Therapy Technologists focus on processing and preparing cell-based therapies in specialized settings, often requiring specific certifications. Laboratory Technicians have a broader role across various lab types, with less emphasis on cell therapy-specific tasks. Both roles are essential in laboratory operations but serve different industry needs.

What skills and qualifications are needed to be a cell therapy technologist?

To thrive as a Cell Therapy Technologist, you need a solid background in biology, laboratory techniques, and quality control, typically supported by a bachelor's degree in a life science or medical laboratory technology. Familiarity with aseptic techniques, Good Manufacturing Practices (GMP), and laboratory information management systems (LIMS) is crucial. Attention to detail, strong communication, and teamwork skills help ensure accuracy and effective collaboration in regulated environments. These skills and qualities are vital for producing safe, high-quality cell therapy products that meet strict regulatory standards.
More about Cell Therapy Technologist jobs
What cities are hiring for Cell Therapy Technologist jobs? Cities with the most Cell Therapy Technologist job openings:
What states have the most Cell Therapy Technologist jobs? States with the most job openings for Cell Therapy Technologist jobs include:
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Cell Therapy Technologist jobs near you
Infographic showing various Cell Therapy Technologist job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 58% Full Time, 21% Part Time, and 17% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $36,219 per year, or $17.4 per hour.

Cell Therapy Manufacturing Specialist

Kelly Services

South San Francisco, CA

$38.50 - $40/hr

Full-time, Contractor

Medical, Dental, Vision, Life, Retirement

Re-posted 15 days ago

Job description

Cell Therapy Manufacturing Specialist
Kelly® Science & Clinical is seeking a Cell Therapy Manufacturing Specialist for a full-time, 6 month contract position at a cutting-edge client in South San Francisco, CA. If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
Pay: $35-38.5/hr AM shifts. $38.5-40/hr for PM shifts
Schedule:
7:00am - 7:30pm?????Sunday - Tuesday; Alternating Wednesday
7:00am - 7:30pm?????Thursday - Saturday; Alternating Wednesday
7:00pm-7:30am??????Sunday - Tuesday; Alternating Wednesday
7:00pm-7:30am??????Thursday - Saturday; Alternating Wednesday
 
Overview
Our client is an industry-leading company that's leading the way in advanced cell therapy manufacturing platforms and process sciences. This innovative organization is at the forefront of developing next-generation cell therapy solutions and is growing rapidly within the biotech/biopharma space.
In this role, you will support manufacturing operations and day-to-day lab operations, with hands-on training across Process Development, Analytical Development, and/or MSAT prior to joining the Manufacturing Group. You will execute manufacturing processes in both R&D and GMP environments, contribute to technical presentations, and play a key role in ensuring compliance with established procedures and quality standards.
Responsibilities:
  • Perform routine procedures following written instructions, including SOPs, batch records, solution documents, and protocols
  • Execute manufacturing processes in both R&D and GMP environments, following protocols and standard operating procedures (SOPs)
  • Provide user feedback to engineering and process teams; support requirements gathering and review
  • Support reagent preparation, leukopak processing, and sample testing in R&D and GMP environments
  • Contribute to the analysis and presentation of technical results at departmental meetings
  • Perform routine clean room and laboratory activities including ordering, cleaning, restocking, and equipment qualification/maintenance
  • Operate in a controlled GMP environment and perform gowning per procedure
  • Complete required training and ensure compliance with established internal and external control procedures
  • Assist in the execution of process, equipment, and cleaning validation
  • Revise and originate production records, standard operating procedures, protocols, and reports
  • Initiate and support the closure of Deviation Reports and CAPAs
  • Train and mentor new manufacturing associates on procedures, aseptic techniques, equipment, and troubleshooting skills
  • Review in-process and completed documents for accuracy and ensure batch records are submitted to area management within specified timeframes
  • Collaborate with Quality Control, Facilities, Materials Management, Quality Assurance, and Validation teams to complete assignments
  • Perform other duties as assigned
Qualifications:
  • Bachelor's Degree or diploma in a scientific or related field is required
  • 1+ years of experience within the biotech/biopharma industry in cGMP Operations, preferably within cell and gene therapy
  • Must know and follow job safety procedures, attend required health and safety training, proactively promote safety at work, and promptly report actual and potential accidents and injuries
  • Must comply with the safety policies of the client and site
  • Adherence to cGMPs is required at all times during the manufacturing of Cell Therapy products
  • Proficiency in Drug Product-related process equipment
  • Must have experience following protocols, SOPs, and/or GMP documentation
  • Excellent verbal, written, presentation, and interpersonal skills
  • Strong analytical and problem-solving skills
  • Self-motivated and passionate about advancing the field of cell therapy
  • Demonstrates self-awareness, integrity, authenticity, and a growth mindset
  • Desire to be part of a rapidly evolving organization, with compelling technology, and take products and processes to the next level
What happens next:
Once you apply, you'll proceed to next steps if your skills and experience look like a good fit. But don't worry – even if this position doesn't work out, you're still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.
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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.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.