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Cell Therapy Process Development Jobs in Texas (NOW HIRING)

Marmon

Process Development Engineer

Harlingen, TX

Process audits to assure correct regrind percentage, cell setup, and processing parameters are in ... Process Development Responsibilities: Perform new process development, including, but not limited ...

Lonza

Manufacturing Supervisor - Cell Therapy

Houston, TX · On-site

$57K - $78K/yr

... development. * Demonstrate technical leadership in cGMP compliance, deviation initiation and ... Solid understanding of production process flow, batch documentation, and quality systems in a ...

Lonza

Manufacturing Supervisor - Cell Therapy

Houston, TX · On-site

$57K - $78K/yr

... development. * Demonstrate technical leadership in cGMP compliance, deviation initiation and ... Solid understanding of production process flow, batch documentation, and quality systems in a ...

Lonza

Core Technician- Cell Therapy 3rd Shift

Houston, TX · On-site

$18.25 - $24/hr

Core Technician - Cell Therapy Location: This is an on-site position located in Houston, TX. As a ... This position is responsible for performing aseptic cell processing activities, operating ...

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Cell Therapy Process Development information

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.

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

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 are popular job titles related to Cell Therapy Process Development jobs in Texas?

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

What job categories do people searching Cell Therapy Process Development jobs in Texas look for?

The top searched job categories for Cell Therapy Process Development jobs in Texas are:

What cities in Texas are hiring for Cell Therapy Process Development jobs?

Cities in Texas with the most Cell Therapy Process Development job openings:

Cell Therapy Process Development jobs near you
Infographic showing various Cell Therapy Process Development job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution.

Research Intern - Cell Therapy Institute

Houston, TX • On-site

MD Anderson
Health Care and Social Assistance • 10K+ employees
Learn more about MD Andersonexternal

Internship

Re-posted 11 days ago

MD Anderson Cancer Center rating

8.5

Company rating: 8.5 out of 10

Based on 172 frontline employees who took The Breakroom Quiz

Job description

Cell therapy is rapidly expanding, with a growing number of innovative programs emerging across both academic institutions and industry. The development of successful cell therapy products is inherently complex, requiring close integration of multidisciplinary expertise toward a shared goal. Our program has demonstrated sustained leadership in the field through the development of pioneering therapies, including virus-specific CTLs and a groundbreaking CAR NK platform. Today, we are recognized as global leaders in the clinical development and application of CAR-NK therapies for cancer treatment.
The research intern will gain hands-on experience in analyzing experimental data related to NK cell function, including cytotoxicity assays such as real-time imaging platforms and Chromium-51 (Cr51) release assays. The intern will be exposed to a broad range of immunotherapy research techniques and will develop foundational knowledge in flow cytometry, specimen processing, and data interpretation. The intern will attend weekly laboratory and journal club meetings, actively engage in question-and-answer discussions, and interact with scientists, clinicians, and researchers across multidisciplinary teams within the Cell Therapy Institute.
All duties and responsibilities are carried out in compliance with institutional policies, ethical research standards, and applicable federal and state regulations.
LEARNING OBJECTIVES
The intern will critically review scientific literature related to immunotherapy and cell therapy research, participate in scientific discussions, and contribute meaningfully during laboratory meetings and collaborative sessions. The experience will also provide training in scientific communication and writing, including data presentation and manuscript-style reporting.
ELIGIBILITY REQUIREMENTS
• Bachelor's or master's degree (recently obtained, typically within one year)
• Prior research experience
• Strong organizational, analytical, and communication skills
Preferred:
• Interest in oncology, clinical research, or academic medicine
• Experience with data analysis or scientific writing
POSITION INFORMATION
Offsite work arrangements are subject to approval and may be modified or revoked at any time based on business needs, performance considerations, or regulatory requirements.
This position may be responsible for maintaining the security and integrity of critical infrastructure, as defined in Section 113.001(2) of the Texas Business and Commerce Code and therefore may require routine reviews and screening. The ability to satisfy and maintain all requirements necessary to ensure the continued security and integrity of such infrastructure is a condition of hire and continued employment.
It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunity without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, disability, protected veteran status, genetic information, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. http://www.mdanderson.org/about-us/legal-and-policy/legal-statements/eeo-affirmative-action.html

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