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Cell Therapy Process Development Jobs (NOW HIRING)

Gilead Sciences, Inc.

Process Engineer III

Santa Monica, CA · On-site

$115K - $149K/yr

Conduct cell therapy process development experiments using automated platforms. * Design and execute laboratory studies that support the evaluation, development and implementation of new technologies ...

Kite Pharma

Process Engineer III

Santa Monica, CA · On-site

$115K - $149K/yr

Conduct cell therapy process development experiments using automated platforms. * Design and execute laboratory studies that support the evaluation, development and implementation of new technologies ...

AstraZeneca

Process Engineer

Rockville, MD · On-site

This position will report to Director, MS&T, Cell Therapy Development and Operations. Key Responsibilities Site manufacturing support • Process Execution Support: Provide day-to-day technical ...

AstraZeneca

Process Engineer

Rockville, MD

This position will report to Director, MS&T, Cell Therapy Development and Operations. Key Responsibilities Site manufacturing support Process Execution Support: Provide day-to-day technical support ...

AstraZeneca

Process Engineer

Rockville, MD · On-site

This position will report to Director, MS&T, Cell Therapy Development and Operations. Key Responsibilities Site manufacturing support • Process Execution Support: Provide day-to-day technical ...

AstraZeneca

Process Engineer

Rockville, MD

The ideal candidate brings hands-on experience with cell therapy unit operations throughpreviousexperience in process development and/or manufacturing, as well asexpertisein technology transfer.

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

As of Jun 7, 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.
Scientist, Process Development

Scientist, Process Development

Cabaletta Bio Inc.

Philadelphia, PA • On-site

Full-time

PTO

Posted 6 days ago

Job description

Scientist, Process Development
Philadelphia, PA
Cabaletta Bio (Nasdaq: CABA) is a clinical-stage biotechnology company focused on developing and launching the first curative targeted cell therapies designed specifically for patients with autoimmune diseases. The CABA™ platform encompasses two complementary strategies which aim to advance the discovery and development of engineered T cell therapies with the potential to become deep and durable, perhaps curative, treatments for a broad range of autoimmune diseases. The lead CARTA (Chimeric Antigen Receptor T cells for Autoimmunity) strategy is prioritizing the development of rese-cel, a 4-1BB-containing fully human CD19-CAR T cell investigational therapy. Rese-cel is currently being evaluated in the RESET™ (REstoring SElf-Tolerance) clinical development program spanning multiple therapeutic areas, including rheumatology, neurology and dermatology. Cabaletta Bio's headquarters and labs are located in Philadelphia, PA. For more information, please visit www.cabalettabio.com
and connect with us on LinkedIn.
Uniquely Differentiated. Rapid. Elegant.
At Cabaletta, we are driven by the shared mission of developing cures, where a patients' own cells are used to fight disease. We are building a culture grounded in the knowledge that successful cures can be achieved for patients if every member of the Cabaletta is focused on the success of the team. To nurture this, we make an active commitment to the well-being and continuous growth of each employee who joins the team. In this way, we are not only working to improve the lives of patients, but of everyone involved. #CabalettaCrew.
We're proud to be a Great Place to Work-Certified™ company! #GPTWcertified Check out what our employees say makes working here so great: Working at Cabaletta Bio Inc | Great Place to Work®
Position Description:
This role is located in Center City, Philadelphia.
Reporting to the Associate Principal Scientist, Process Development, the Scientist, Process Development will lead the refinement, development, and characterization of cell therapy processes, and support the transfer of product candidates to Cabaletta's external manufacturing partners (CDMOs). This role partners closely with cross-functional teams including MSAT, Analytical Development, Preclinical, Quality, CMC, and Regulatory to enable robust, scalable, and compliant manufacturing processes. The position may require up to 10% domestic travel, as well as occasional weekend or extended-hour support during critical activities such as tech transfer or manufacturing campaigns.
Responsibilities
  • Design and execute process development experimental plans, author associated protocols and reports, and present data and insights to cross-functional teams.
  • Develop phase-appropriate cell therapy manufacturing processes using Quality by Design (QbD) principles.
  • Support technology transfer of processes to CDMOs for early-phase cGMP clinical manufacturing, as needed.
  • Contribute to the development of platform manufacturing processes and ensure readiness for clinical and future commercial manufacturing.
  • Identify and evaluate opportunities to improve manufacturing performance, including cost, throughput, robustness, and quality.
  • Maintain laboratory materials and sample inventory to support experimental planning and execution.
  • Accurately document experimental data in a timely manner, ensuring data integrity, traceability, and compliance with protocols.
  • Maintain individual training requirements in a compliant state.
  • Contribute to regulatory filings (e.g., IND/CTA) and technical documentation, as needed.
  • Other related duties, as assigned

Qualifications:
  • Bachelors Degree with 4 + years experience or Masters Degree with 2 + years' experience within biologics process development and manufacturing under cGMP processes.
  • Experience with cell therapy manufacturing scale up, technology transfer, and process development methods, scale-up, and tech transfer methods is required.
  • Experience of basic biological laboratory techniques such as cell culture, PCR, cell-based bioassays, and/or ELISA.
  • Extensive flow cytometry experience is required.in flow cytometry and cell-based assays.
  • Strong problem-solving skill is preferred.
  • Experience supporting documents for regulatory review including but not limited to INDs, CTAs, and BLAs.
  • Previous experience and working knowledge of T-cells or immunological cell therapies.
  • Good working knowledge in cGMP manufacturing of biological process and ICH regulations.
  • Highly organized and efficient, with a curiosity to be part of cutting-edge science.
  • Strong team orientation and passion for continuous self-development.
  • Ability to coordinate parallel tasks across multiple projects, demonstrating prioritization.

Our name - Cabaletta - is derived from the operatic term that represents a rapid, repetitive, and technically challenging section of an operatic aria, designed to showcase the skills of the lead singer. Analogously, Cabaletta Bio strives to achieve rapid and repetitive product development, building on our indication prioritization and biologic platform that targets the driver of specific autoimmune diseases without the need for long-term immunosuppression.
For more information, please visit https://www.cabalettabio.com/join-our-crew
Our most important asset is our people, and we offer competitive benefits, PTO, and stock option plans.
Cabaletta Bio is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability, protected veteran status or any other basis protected by applicable law.
Cabaletta Bio, Inc. does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with Cabaletta, a Master Services Agreement (MSA) must be executed and confirmed prior to submitting any information relating to a potential candidate. Without a signed MSA, Cabaletta shall not be responsible to any individual or entity for any payment relating to any form of fee or compensation.
And, if a resume or candidate is submitted by a recruiter, an employment agency, or a staffing firm without a fully executed MSA, Cabaletta has the unrestricted right to pursue and hire any of those candidate(s) without any legal or financial responsibility to the recruiter, agency, and/or firm.
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