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Cell Therapy Process Development Jobs in California

AstraZeneca

Lead Cell Therapy Specialist

Los Angeles, CA · On-site

$81K - $122K/yr

Skilled at working effectively across Manufacturing, Quality, MSAT, Process Development, Supply ... Cell therapy expertise : Priority experience in cell therapy manufacturing * Manufacturing ...

Moffitt

CELL THERAPY TECHNOLOGIST I

Long Beach, CA

$16.25 - $21/hr

The Cell Therapy Technologist I is required to document each step of a process and/or procedure per the facility's standard operating procedures and policies. The Cell Therapy Technologist I complies ...

Bayer

$22 - $24.50/hr

You collaborate closely with Biological Development (BD) and Manufacturing Science and Technology ... In this role, you act as the technical SME for key aspects of the manufacturing process and help ...

Astrazeneca

Lead Cell Therapy Specialist

Los Angeles, CA · On-site

$81K - $122K/yr

Skilled at working effectively across Manufacturing, Quality, MSAT, Process Development, Supply ... Cell therapy expertise : Priority experience in cell therapy manufacturing * Manufacturing ...

Cellares

Process Engineer

South San Francisco, CA · On-site

$90K - $210K/yr

Position Summary We are seeking an innovative and highly motivated Process Engineer to join the MSAT team who will contribute significantly to the development of our advanced cell therapy ...

Cellares

Process Engineer

South San Francisco, CA · On-site

Position Summary We are seeking an innovative and highly motivated Process Engineer to join the MSAT team who will contribute significantly to the development of our advanced cell therapy ...

Cellares

Process Engineer

South San Francisco, CA · On-site

Position Summary We are seeking an innovative and highly motivated Process Engineer to join the MSAT team who will contribute significantly to the development of our advanced cell therapy ...

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Cell Therapy Process Development information

What are the key skills and qualifications needed to thrive as a cell therapy process development professional?

To thrive in Cell Therapy Process Development, you need a solid background in cell biology, biotechnology, or a related field, often supported by a relevant degree and experience with cell culture techniques. Familiarity with bioprocessing equipment, Good Manufacturing Practice (GMP) regulations, and analytical tools such as flow cytometry and PCR is typically required. Strong problem-solving skills, attention to detail, and effective teamwork enhance performance in this collaborative and innovative environment. These competencies ensure the safe and efficient development of cell therapies, meeting rigorous quality standards and advancing clinical applications.

What are some typical challenges faced by professionals in cell therapy process development, and how are they addressed?

Professionals in Cell Therapy Process Development often encounter challenges such as scaling up production processes from laboratory to clinical or commercial scale while maintaining product quality and consistency. Additional hurdles include adhering to strict regulatory requirements and managing complex collaborations across cross-functional teams, like quality assurance, regulatory affairs, and manufacturing. These challenges are typically addressed through rigorous process optimization, thorough documentation, and ongoing communication with stakeholders to ensure that all aspects of the process meet industry standards and regulatory expectations.

What is the difference between Cell Therapy Process Development vs Cell Therapy Manufacturing Specialist?

AspectCell Therapy Process DevelopmentCell Therapy Manufacturing Specialist
CredentialsTypically requires a degree in biology, biochemistry, or biomedical engineering; certifications in GMP or cell therapy are commonSimilar credentials; often holds degrees in related fields and GMP certifications
Work EnvironmentResearch labs, development facilities, early-stage process optimizationManufacturing plants, production floors, quality control labs
Industry UsageFocuses on developing and optimizing cell therapy processesInvolved in large-scale production and process execution

Cell Therapy Process Development professionals focus on designing and refining cell therapy procedures, while Cell Therapy Manufacturing Specialists handle the production and quality assurance in manufacturing settings. Both roles require similar educational backgrounds and certifications but differ mainly in their work environment and specific responsibilities.

What is cell therapy process development?

Cell Therapy Process Development refers to the design, optimization, and scaling up of manufacturing processes for cell-based therapies, such as CAR-T cells or stem cell products. Professionals in this field work on translating laboratory research into reproducible, efficient, and safe production methods that meet regulatory standards. This involves working with cell culture techniques, bioreactors, quality control, and process validation to ensure that therapies can be produced consistently for clinical and commercial use. The goal is to develop robust processes that deliver safe and effective cell therapies to patients.
What are popular job titles related to Cell Therapy Process Development jobs in California? For Cell Therapy Process Development jobs in California, the most frequently searched job titles are:
What job categories do people searching Cell Therapy Process Development jobs in California look for? The top searched job categories for Cell Therapy Process Development jobs in California are:
What cities in California are hiring for Cell Therapy Process Development jobs? Cities in California with the most Cell Therapy Process Development job openings:
Cell Therapy Process Development jobs near you
Infographic showing various Cell Therapy Process Development job openings in California as of August 2026, with employment types broken down into 61% Full Time, and 39% Part Time. Highlights an 100% In-person job distribution.

Cell Therapy Manufacturing Specialist

Kelly Services

South San Francisco, CA

Full-time, Other

Medical, Dental, Vision, Life, Retirement

Re-posted 17 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.
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