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How much do cell therapy process development jobs pay per hour?

As of Jun 6, 2026, the average hourly pay for cell therapy process development in the United States is $33.68, according to ZipRecruiter salary data. Most workers in this role earn between $27.64 and $41.35 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Cell Therapy Process Development professional, and why are they important?

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.
Infographic showing various Cell Therapy Process Development job openings in the United States as of May 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 90% Full Time, 2% Part Time, and 6% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $70,060 per year, or $33.7 per hour.

Senior Scientist, Cell Therapy Process Development

GeneFab

Alameda, CA

$103K - $141K/yr

Full-time

Posted 9 days ago

Job description

GeneFab is seeking a highly skilled Senior Scientist to join our Cell Therapy Process Development team in Alameda, CA. In this role, you will lead the design and optimization of integrated processes, bridging the gap between innovative synthetic biology and phase-appropriate cGMP manufacturing. If you have hands-on experience with automated cell processing and a passion for driving clinical readiness for next-generation genetic medicines, we want to hear from you.
Responsibilities:

  • Design and perform experiments to optimize integrated processes for cell therapy, including: evaluation of cell sources, isolation and activation of human immune cells, media optimization, viral/non-viral genetic modification, cell expansion, cell harvest/fill/finish, and cryopreservation. 

  • Cell therapy process scaleup, including: transition from open processes to closed automated systems, understanding analytical methods, using a Design of Experiments (DoE) approach, and evaluating process choices within a Quality by Design (QbD) framework 

  • Exploration of new technologies or materials for process scale-up or improvements with quality mindset leading to clinical or commercial readiness.  

  • Cross-functional collaborations in project teams to translate scientific understanding to development of phase appropriate cGMP cell therapy manufacturing unit operations. 

  • Lead the design, execution, and analysis of experimental studies for new manufacturing technologies and processes 

  • Author and review study protocols, technical reports, ELNs, regulatory submissions. 

  • Support authoring of key documentation to enable technology transfer (e.g. sampling plans, batch records, specifications, SOPs, FMEA, flow diagrams, etc.). 

  • Help coordinate sample management workflow across Process and Analytical Development teams and manage development database 

  • Serve as a technical resource/SME for GMP operations (e.g. root cause analyses and continuous improvement initiatives) 

  • Coordinate and prioritize tasks across multiple projects 

  • Maintain familiarity with current state-of-the-art related to cell therapy processes 

Qualifications:

  • BS/MS with 6+ years or PhD with 4+ years of experience in science/engineering of biopharmaceutical or cell/gene therapy process development and technology transfer  

  • Hands-on experience with automated cell processing units or platforms (i.e. bioreactors, automated cell wash, fill and finish) is critical.  

  • Experience developing and optimizing cell therapy processes for GMP production with quality mindset  

  • Strong technical writing and communication skills to support both development and tech transfer applications 

  • Strong critical thinking, organizational skills, ability to work in multi-functional project teams, and attention to detail  

  • Experience with various types of cell therapy products (i.e. CAR-T, CAR-NK, HSC, MSC) is preferred 

  • Experience with AI solutions for CGT processes and working with LIMS is a plus  

About GeneFab 
GeneFab is a contract manufacturing and synthetic biology biofoundry focused on cell and gene therapies. GeneFab was formed in 2023 with a vision to combine industry leading expertise in synthetic biology with advanced cGMP capabilities in order to accelerate the development and commercialization of genetic medicines. GeneFab offers its customers an extensive technology platform and know-how that spans early stage product design, technical development, and cGMP compliant production. GeneFab's technology platform includes bioinformatic-guided discovery of cell type promoters, directed evolution of small molecule-regulated gene switches, and the engineering of highly sensitive kill switches for enhanced safety and control of cellular therapies.

We are committed to an inclusive and diverse GeneFab. We believe that different perspectives lead to better ideas, and better ideas allow us to better understand the needs and interests of our diverse GeneFab team. We welcome people of different backgrounds, experiences, abilities, and perspectives and are an equal opportunity employer.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.