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Cell Therapy Process Development Engineer Jobs (NOW HIRING)

Legend Biotech USA, Inc.

Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy ... Role OverviewThe Senior Engineer / Principal Engineer, Lentivirus Downstream Process Development ...

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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 Sep 13, 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 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.

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

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 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 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 popular job titles related to Cell Therapy Process Development Engineer jobs?

For Cell Therapy Process Development Engineer jobs, the most frequently searched job titles are:

Infographic showing various Cell Therapy Process Development Engineer job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 81% Full Time, 15% Part Time, and 2% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $101,612 per year, or $48.9 per hour.

Process Engineer II Cell Therapy Process Development

Walnut Park, CA • On-site

Cube Hub, Inc.
Recruiting and Staffing Services • 11 - 50 employees
Learn more about Cube Hub, Inc.external

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Dental, Vision

Posted 2 days ago

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Job description

Job Title: Process Engineer II Cell Therapy Process Development

Location: Santa Monica, CA Onsite 5 Days/Week
Schedule: Monday Friday, 9:00 AM 5:00 PM; occasional weekends based on business needs
Duration: 12-Month Contract
Contract Type: Contract; potential for conversion based on business needs

Job Summary

Our client is seeking a highly motivated and detail-oriented Process Engineer II with hands-on process development experience to support innovative T-cell therapies for cancer treatment.

This position will be part of the Autologous Process Design and Development Life Cycle Management Team and will support process development, process characterization, technology transfer, and continuous improvement activities for cell therapy products.

The successful candidate will design and execute laboratory experiments, analyze and present data, support manufacturing process improvements, and develop technical documentation for clinical and commercial manufacturing.

Key Responsibilities

  • Design and execute cell therapy process development experiments using automated platforms.
  • Conduct laboratory studies to evaluate and implement new technologies, materials, and processes.
  • Perform hands-on activities in a cell culture laboratory, including cell passaging, sampling, fluid handling, media preparation, reagent management, and cryopreservation.
  • Support process and equipment characterization, performance monitoring, and trending.
  • Develop and improve manufacturing equipment and systems for cell therapy products, including hardware, software, single-use components, and user requirements.
  • Evaluate new technologies and materials for implementation into GMP manufacturing.
  • Support technology transfer activities and GMP manufacturing operations.
  • Provide process training to GMP manufacturing personnel.
  • Apply Design of Experiments (DOE) and statistical analysis to support process development and optimization.
  • Utilize tools such as JMP and/or Minitab for statistical analysis.
  • Prepare and review protocols, SOPs, manufacturing batch records, technical reports, and summary reports.
  • Analyze experimental data and communicate conclusions and recommendations to cross-functional teams.
  • Create and present technical presentations and data summaries to project teams, senior leadership, and external collaborators.
  • Troubleshoot process and equipment issues and recommend timely solutions.
  • Collaborate with Research, Development, Manufacturing, Quality, and other cross-functional teams.
  • Perform other duties as assigned.

Required Qualifications

  • MS degree in Biochemical Engineering, Chemical Engineering, Biomedical Engineering, Biotechnology, or related discipline with 2+ years of pharmaceutical/biotechnology manufacturing or process development experience; OR
  • BS degree in a related engineering or biotechnology discipline with 4+ years of relevant experience; OR
  • AS degree in a related discipline with 5+ years of relevant experience; OR
  • High School diploma with 6+ years of pharmaceutical/biotechnology manufacturing or process development experience.

Required Experience

  • Hands-on experience in cell therapy process development.
  • Experience working with automated cell therapy/cell processing platforms.
  • Hands-on cell culture and aseptic processing in an ISO 5 environment.
  • Experience with cell passaging, sampling, fluid handling, media formulation, reagent management, and cryopreservation.
  • Practical experience with bioreactors and bioprocess development.
  • Experience designing and executing Design of Experiments (DOE).
  • Working knowledge of statistical analysis and process data evaluation.
  • Practical knowledge of cGMP manufacturing and applicable pharmaceutical/biotechnology regulations.
  • Understanding of bioprocessing principles including scale-up/scale-out, hydrodynamics, mass transfer, and bioreactor design and monitoring.
  • Understanding of cell biology, cell populations/subtypes, differentiation, phenotype markers, and metabolic pathways.
  • Knowledge of material science and material compatibility for cell culture applications.
  • Experience with biotechnology product manufacturing, aseptic processing, cell therapy, and process development.
  • Strong troubleshooting, critical-thinking, and problem-solving skills.
  • Excellent written and verbal communication skills.
  • Ability to work independently in a fast-paced and changing environment.
  • Ability to collaborate effectively across Research, Development, Manufacturing, and other cross-functional teams.

Preferred Qualifications

  • Experience with T-cell therapy or CAR-T manufacturing/process development.
  • Experience with autologous cell therapy.
  • Experience with automated cell processing technologies.
  • Experience with flow cytometry.
  • Experience with mRNA handling and processing.
  • Experience with single-use technologies and disposable systems.
  • Experience with JMP or Minitab.
  • Experience supporting technology transfer into GMP manufacturing.

Work Environment

  • 100% onsite in Santa Monica, CA
  • Monday Friday, 9:00 AM 5:00 PM
  • Occasional weekend work may be required based on business needs.
  • This is a 12-month contract position, with potential for conversion depending on business needs and performance.

Company Description:
Cube Hub knows that you want to be a valuable and valued employee to useyour skills, be challenged and contribute. We get it, and we make that happen for you. Cube Hub wants you to shine, so we place you in a job that matches your experience, your skills, and your concept of the ideal workplace. We also offer a competitive compensation package a salary based on your experience, skills, and location, and a comprehensive suite of healthcare/Dental/Vision and other benefits for more details visit: . With Cube Hub, you get more than an assignment. You get a career. After placing you on assignment, your Cube Hub recruiter gets to work finding your next engagement. Our colossal year- over-year growth unlocks doors of opportunity to keep you employed and on the path of professional growth. Join our team and get started on a career that recognizes who you are and what you have to offer. "Cube Hub is an Equal Opportunity Employer and does not discriminate in employment on the basis of Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans

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