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Cell Therapy Process Development Engineer Jobs (NOW HIRING)

Kite Pharma

Process Engineer II- MSAT

Frederick, MD · On-site

$99K - $129K/yr

This role will provide process engineering support for the validation and commercial manufacturing of cell therapy products.Working cross functionally with quality, operations, process development ...

Huntsman

Process Development Engineer

Mcintosh, AL · On-site

: Process Development Engineer Huntsman is seeking a Process Development Engineer supporting the ADMAT Division located at the McIntosh Site . This position will report to the Site PD Manager . Job ...

SpaceX

Process Development Engineer

Hawthorne, CA

$110K - $135K/yr

PROCESS DEVELOPMENT ENGINEER - BUILD RELIABILITY The Process Development Engineer is responsible for developing and improving business processes and systems that enable SpaceX to design, build ...

SpaceX

Process Development Engineer

Hawthorne, CA

$110K - $135K/yr

PROCESS DEVELOPMENT ENGINEER - BUILD RELIABILITY The Process Development Engineer is responsible for developing and improving business processes and systems that enable SpaceX to design, build ...

5AM Ventures

Process Development Engineer

Emeryville, CA

$85K - $125K/yr

In this newly created role, as a Process Development Engineer I, you will work in close collaboration with our Process Development team, and our Senior Process Engineer in particular, to advance our ...

Cellares

Senior Process Engineer

Bridgewater, NJ

$90K - $210K/yr

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

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Cell Therapy Process Development Engineer information

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$45.5K

$101.6K

$152.5K

How much do cell therapy process development engineer jobs pay per year?

As of Jun 7, 2026, the average yearly pay for cell therapy process development engineer in the United States is $101,612.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,500.00 and $119,000.00 per year, depending on experience, location, and employer.

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

AspectCell Therapy Process Development EngineerCell Manufacturing Technician
CredentialsBachelor's or Master's in Biotechnology, Bioengineering, or related fields; experience in cell culture and process developmentHigh school diploma or associate degree; on-the-job training in manufacturing processes
Work EnvironmentLaboratories, R&D settings, process optimization labsManufacturing floors, cleanrooms, production facilities
Industry UsageResearch, process development, scale-up activities in biotech and pharma companiesProduction, batch manufacturing, quality control in cell therapy manufacturing plants

The Cell Therapy Process Development Engineer focuses on developing and optimizing processes in labs, requiring advanced degrees and specialized skills. In contrast, the Cell Manufacturing Technician works on executing manufacturing processes on the production floor, often with less formal education. Both roles are essential in the cell therapy industry but differ in responsibilities, environment, and expertise level.

What are some common challenges faced by Cell Therapy Process Development Engineers when scaling up processes from the lab to clinical or commercial manufacturing?

Cell Therapy Process Development Engineers often encounter challenges when translating small-scale laboratory protocols to large-scale manufacturing, such as maintaining cell viability and product consistency. Ensuring reproducibility, meeting stringent regulatory requirements, and adapting to variations in raw materials are also key obstacles. Collaborating closely with quality assurance, manufacturing, and regulatory teams is vital to address these issues and develop robust, scalable processes that adhere to industry standards.

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

To thrive as a Cell Therapy Process Development Engineer, you need a strong background in biomedical engineering, cell biology, or a related field, often with advanced degrees and experience in cell culture techniques. Familiarity with bioprocessing equipment, automation systems, and regulatory standards such as GMP is typically required, along with knowledge of analytical tools for process characterization. Strong problem-solving skills, attention to detail, and effective collaboration are critical soft skills in this role. These competencies are essential to ensure robust, scalable, and compliant cell therapy manufacturing processes that meet quality and safety standards.

What does a Cell Therapy Process Development Engineer do?

A Cell Therapy Process Development Engineer is responsible for designing, optimizing, and scaling up processes used to manufacture cell-based therapies for clinical and commercial use. They work closely with research scientists, manufacturing teams, and quality assurance to ensure that cell therapy products are produced safely, efficiently, and consistently. Their work often includes developing protocols, troubleshooting production issues, implementing new technologies, and ensuring regulatory compliance in a highly controlled environment.
Infographic showing various Cell Therapy Process Development Engineer job openings in the United States as of May 2026, with employment types broken down into 80% Full Time, and 20% Contract. Highlights an 100% In-person job distribution, with an average salary of $101,612 per year, or $48.9 per hour.
Process Engineer, Process Development

Process Engineer, Process Development

Kyverna Therapeutics

Emeryville, CA • On-site

Full-time

Posted 4 days ago

Job description

Responsibilities
  • Lead design, optimization and technical execution of process development activities for autologous CAR T cell workflows (cell isolation, activation, transduction/transfection, expansion, harvest, formulation, cryopreservation).
  • Develop and implement automated formulation and fill/finish processes for cell therapy drug product, including closed-system and aseptic considerations.
  • Support the integration and validation of robotics platforms with cell processing steps as process subject matter expert.
  • Design experiments, run bench- and pilot-scale studies, maintain accurate lab notebook entries, analyze data, and generate technical reports.
  • Draft and maintain process documentation including process descriptions, process control strategies, bill of materials, and standard operating procedures.
  • Maintain accurate documentation (protocols, batch records, risk assessments, CAPAs) consistent with regulatory and GMP standards.
  • Support technology transfer to MSAT and manufacturing, including development of manufacturing instructions, equipment requirements, training materials, and execution support.
  • Work with analytical development and quality control to define in-process controls, release testing, and associated acceptance criteria.
  • Support equipment qualification, process validation, and troubleshooting in GMP environments.
  • Participate in cross-functional project teams and present technical updates to stakeholders.

Qualifications
  • BS in Chemical, Biomedical, Biological Engineering, or related field and 8 years experience in process development for cell therapy products; direct experience with autologous CAR T highly preferred.
  • MS in Chemical, Biomedical, Biological Engineering, or related field (MS preferred) and 6 years experience in process development for cell therapy products; direct experience with autologous CAR T highly preferred..
  • Practical experience designing and executing cell culture/expansion and formulation processes for cell therapy drug products.
  • Hands-on experience with automation of formulation and fill/finish steps; familiarity with closed-system processing and aseptic fill technologies.
  • Knowledge of GMP requirements, technology transfer practices, and manufacturing support (MSAT).
  • Strong data analysis skills and proficiency with experimental design, statistical analysis, and process characterization.
  • Excellent technical writing skills for protocols, reports, and process transfer packages.
  • Experience with specific automated platforms (e.g., CliniMACS Prodigy, CTS Rotea, CTS Compleo, GatheRex, GE WAVE, Dynaselect) or robotic solutions.
  • Experience integrating robotics and automation systems (e.g., liquid handlers, robotic arms, automated incubators/bioreactors) into bioprocess workflows.
  • Strong problem-solving and troubleshooting capability in laboratory and pilot-scale environments.
  • Collaborative team player with demonstrated ability to work cross-functionally with MSAT, manufacturing, analytical, QA, and RegCMC.
  • Effective communicator-able to present complex technical concepts clearly to scientific and non-scientific stakeholders.
  • Organized, detail-oriented, able to manage multiple priorities and project timelines.
  • Comfortable working in dynamic, fast-paced biotech environments.

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