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Process Engineer Cell Therapy Jobs in Spring, TX

Lonza

Research Associate III

Houston, TX

... Engineering, or related field with 2-4 years of experience in bioprocessing or cell therapy development * Strong hands-on experience with cell therapy manufacturing and process development, including ...

Lonza

Research Associate III

Houston, TX · On-site

... Engineering, or related field with 2-4 years of experience in bioprocessing or cell therapy development * Strong hands-on experience with cell therapy manufacturing and process development, including ...

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Showing results 1-20

All JobsProcess Engineer Cell Therapy JobsProcess Engineer Cell Therapy Jobs in Spring, TX

Process Engineer Cell Therapy information

See Spring, TX salary details

$44K

$81.9K

$126.8K

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

As of Jul 14, 2026, the average yearly pay for process engineer cell therapy in Spring, TX is $81,886.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,300.00 and $91,700.00 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, and why are they important?

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 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.

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 are popular job titles related to Process Engineer Cell Therapy jobs in Spring, TX? For Process Engineer Cell Therapy jobs in Spring, TX, the most frequently searched job titles are:
Process Engineer Cell Therapy jobs near you
Infographic showing various Process Engineer Cell Therapy job openings in Spring, TX as of July 2026, with employment types broken down into 100% Contract. Highlights an 100% In-person job distribution, with an average salary of $81,886 per year, or $39.4 per hour.
Research Associate III

Research Associate III

Lonza

Houston, TX

Full-time

Medical, Dental, Vision, PTO

Posted 13 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

23rd of 74 rated pharmaceutical

Job description

Research Associate III
Location: Pearland, TX, USARelocation assistance is available for eligible candidates and their families, if needed.Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there is no single way of doing things. Our greatest strength is our people working together to develop ideas that help businesses help people. In return, we empower our teams to own their careers and make a meaningful impact on the world.In this role, you will support the development of innovative cell therapy processes by conducting experiments, analyzing results, and contributing to process development activities.What you will get
  • An agile career with opportunities for professional growth
  • A collaborative and inclusive workplace culture
  • Competitive compensation that rewards performance
  • Medical, dental, and vision insurance
  • Generous paid time off and holiday programs
  • Access to learning and development resources
What you will do
  • Bachelor's or master's degree in Bioengineering, Chemical Engineering, or related field with 2-4 years of experience in bioprocessing or cell therapy development
  • Strong hands-on experience with cell therapy manufacturing and process development, including pluripotent stem cells (iPSC), mesenchymal stem cells (MSC), hematopoietic stem cells (HSC), immune cells, and other primary cell types.
  • Demonstrated expertise in closed aseptic processing, including sterile welding, sealing, tubing assemblies, sampling, and contamination control practices. Bioreactor experience is a plus
  • Experience operating single-use bioprocessing equipment and unit operations such as perfusion, continuous centrifugation, automated magnetic cell separation, buffer exchange, and volume reduction.
  • Proficiency in sterile cell culture techniques and routine manipulation of mammalian cell cultures within controlled environments.
  • Experience with GMP documentation, technical writing, strong verbal and written communication skills, and statistical data analysis
  • Ability to manage multiple priorities in a fast-paced environment with strong agility
What we are looking for
  • Strong hands-on experience with cell therapy manufacturing and process development, including pluripotent stem cells (iPSC), mesenchymal stem cells (MSC), hematopoietic stem cells (HSC), immune cells, and other primary cell types.
  • Demonstrated expertise in closed aseptic processing, including sterile welding, sealing, tubing assemblies, sampling, and contamination control practices.
  • Experience operating single-use bioprocessing equipment and unit operations such as perfusion, continuous centrifugation, automated magnetic cell separation, buffer exchange, and volume reduction.
  • Proficiency in sterile cell culture techniques and routine manipulation of mammalian cell cultures within controlled environments.
  • Experience designing experiments, performing statistical data analysis, and interpreting process performance data.
  • Strong technical documentation, data reporting, and presentation skills within regulated development or manufacturing environments.
  • Experience working within cGMP environments and collaborating across Manufacturing, Quality, Analytical, and Project Management functions.
About LonzaAt Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion, and Integrity reflect who we are and how we work together.We are committed to fostering an inclusive workplace and providing equal opportunities to all qualified applicants.Ready to shape the future of life sciences? Apply now.

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