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Process Engineer Cell Therapy Jobs (NOW HIRING)

Gotion, Inc.

Process Engineer - Cell Line

Manteno, IL · On-site

Prefer with the principles of lithium-ion batteries and the cell manufacturing process. * Bachelor's degree or above, majoring in electrochemistry, physical materials, materials engineering, chemical ...

RoslinCT US

Senior Process Engineer

Hopkinton, MA

$114K - $147K/yr

WHO WE ARE We are a leading cell therapy contract development and manufacturing organization ... The Process Engineer will play a key role in optimizing manufacturing processes, ensuring ...

Catalent, Inc.

Process Engineer MS&T

Princeton, NJ · On-site

This role ensures cell therapy processes are robust, scalable, and compliant with cGMP standards. You will drive seamless technology transfer, reliable manufacturing, and continuous improvement to ...

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Process Engineer Cell Therapy information

See salary details

$49.5K

$92K

$142.5K

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

As of Aug 25, 2026, the average yearly pay for process engineer cell therapy in the United States is $92,018.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $103,000.00 per year, depending on experience, location, and employer.

What does a process engineer in cell therapy do?

A Process Engineer in Cell Therapy is responsible for developing, optimizing, and overseeing the manufacturing processes used to produce cell-based therapies. They ensure that processes are efficient, scalable, and compliant with regulatory standards, while maintaining the quality and safety of the final product. Their work often involves collaborating with scientists, quality teams, and production staff to troubleshoot issues and implement improvements. Process Engineers in this field play a crucial role in bringing innovative cell therapies from the laboratory to clinical and commercial production.

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

To thrive as a Process Engineer in Cell Therapy, you need a strong background in chemical or biomedical engineering, experience with cell culture processes, and often a relevant degree. Familiarity with GMP regulations, bioprocessing equipment, and quality control systems is typically required, along with experience using tools like bioreactors and analytical software. Excellent problem-solving, communication, and project management skills help you collaborate effectively and drive process improvements. These skills ensure the development and optimization of safe, scalable, and compliant cell therapy manufacturing processes.

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

Process Engineers in Cell Therapy often encounter challenges such as scaling up production from clinical to commercial scale while maintaining stringent quality standards and regulatory compliance. Managing variability in biological materials and ensuring consistency across batches is another common hurdle. These challenges are typically addressed through robust process development, close collaboration with quality and manufacturing teams, and implementation of automation and data-driven process controls. Continuous training and adaptation to evolving regulatory guidelines also play a key role in overcoming these obstacles.

What is the difference between Process Engineer Cell Therapy vs Process Engineer Bioprocess?

AspectProcess Engineer Cell TherapyProcess Engineer Bioprocess
CredentialsBachelor's/Master's in Bioengineering, Chemical Engineering, or related fieldsBachelor's/Master's in Bioengineering, Chemical Engineering, or related fields
Work EnvironmentCell therapy manufacturing facilities, GMP labsBiopharmaceutical production plants, GMP facilities
Industry UsageCell therapy companies, biotech firmsBiotech, pharmaceutical manufacturing
Common Search/ComparisonYesYes

Process Engineer Cell Therapy and Process Engineer Bioprocess roles share similar educational backgrounds and work environments, often within GMP manufacturing settings. The main difference lies in their focus: cell therapy engineers specialize in developing and scaling processes for cellular treatments, while bioprocess engineers work on broader biopharmaceutical production. Both roles are essential in biotech industries and often overlap in skills and certifications.

More about Process Engineer Cell Therapy jobs

What cities are hiring for Process Engineer Cell Therapy jobs?

Cities with the most Process Engineer Cell Therapy job openings:

What states have the most Process Engineer Cell Therapy jobs?

States with the most job openings for Process Engineer Cell Therapy jobs include:

What job categories do people searching Process Engineer Cell Therapy jobs look for?

The top searched job categories for Process Engineer Cell Therapy jobs are:

Process Engineer Cell Therapy jobs near you
Infographic showing various Process Engineer Cell Therapy job openings in the United States as of July 2026, with employment types broken down into 100% Contract. Highlights an 100% In-person job distribution, with an average salary of $92,018 per year, or $44.2 per hour.

Process Engineer - Cell & Gene Therapy

Boston, MA • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

Contractor

Re-posted 20 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Process Engineer – Cell & Gene Therapy position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Position: Process Engineer – Cell & Gene Therapy

Location: Boston, MA or Providence, RI (Onsite)
Duration: 12-Month Contract (Extension Potential)

Job Overview

We are seeking a Process Engineer to support innovative Cell & Gene Therapy manufacturing projects. This role will focus on implementing manufacturing equipment and automated process systems while driving process optimization, validation, and continuous improvement initiatives within a GMP environment.

Key Responsibilities

  • Lead equipment implementation from design through commissioning, qualification, and validation.
  • Support automation projects, process optimization, and manufacturing system improvements.
  • Execute FAT, SAT, commissioning, and startup activities.
  • Troubleshoot process and equipment issues to improve manufacturing performance.
  • Support technology transfer, CAPAs, change controls, and deviation investigations.
  • Collaborate with Manufacturing, MSAT, Validation, Quality, and Engineering teams to ensure successful project execution.

Required Qualifications

  • Bachelor's degree in Engineering or a related technical field.
  • Experience in Cell & Gene Therapy, Biopharmaceutical, or Pharmaceutical Manufacturing.
  • Hands-on experience with process engineering, equipment implementation, and GMP manufacturing.
  • Knowledge of commissioning, qualification, validation, FAT/SAT, and technology transfer activities.
  • Experience with automation systems and continuous process improvement.
  • Strong troubleshooting, communication, and cross-functional collaboration skills.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com