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Cell Therapy Process Development Jobs in Texas (NOW HIRING)

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 ...

CTMC

Director, Business Development

Houston, TX · On-site

$180 - $230/hr

Our mission is to accelerate cell therapies from bench to bedside. We offer development and ... and processes to deliver exceptional results. Our state-of-the-art, 60,000 sq. ft. industrial ...

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Cell Therapy Process Development information

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 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 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 70% Full Time, and 30% Part Time. Highlights an 100% In-person job distribution.

Postdoctoral Fellow - Cell Therapy Institute

MD Anderson

Houston, TX • On-site

$46K - $63K/yr

Other

Re-posted 27 days ago

MD Anderson Cancer Center rating

8.4

Company rating: 8.4 out of 10

Based on 170 frontline employees who took The Breakroom Quiz

24th of 887 rated healthcare providers

Job description

A postdoctoral fellow position is available in the department of Cell Therapy Institute. The primary purpose of the Postdoctoral Fellow is to assist the Principal Investigator and other Faculty members with scientific research projects within the Institute for Cell Therapy Discovery and Innovation. The primary activity of this position is with a team of cancer immunotherapy lab researchers.

We seek a postdoc position focused on developing lipid nanoparticle for in vivo delivery of mRNA for cancer and other human disease. We are a fast-paced and collaborative team working on CAR NK/T based cancer immunotherapy in clinical trials. This position will primarily lead to the use of proprietary LNP formulation and conjugation technology to deliver and target different cell types specifically in human patients.

You will seal the gap between LNP-mRNA-based targeting and our CAR NK immunotherapy. The applicants should have a deep understanding of lipid chemistry, hands-on laboratory work with lipid nanoparticle, lipid toxicity, LNP formulation, characterization, functionality assay in vitro and in vivo. Cell Therapy is expanding with numerous cell projects being developed by academic centers and industry.

The development of a cell therapy product is complex and requires integration of multiple disciplines with a common purpose. We have proven our capacity for leadership in the field of cell therapy by developing novel therapies such as viral CTLs and a CAR NK program. We are currently world leaders in the use of CAR-NK to treat cancer All duties and responsibilities are carried out in compliance with institutional policies, ethical research standards, and applicable federal and state regulations.

LEARNING OBJECTIVES Formulation and conjugation of lipid nanoparticles In vitro screening of delivery systems work closely with other members in the lab on cell culture and mouse studies. Maintain detailed records of analytical data Interface directly with other functional teams Work independently and collaboratively to drive design, functional screening, development and production of novel tLNP formulations for targeted in vivo delivery ELIGIBILITY REQUIREMENTS PhD degree in chemistry, biochemistry, or bioengineering with experience on LNP design and delivery. Demonstrated ability with respect to successful designed, formulation, and test for LNP functionality and toxicity.

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 Apply

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