Intern, Manufacturing

Company: CTMC
Location: Houston
Posted on: February 17, 2026

Job Description:

Job Description Job Description Location: Houston, TX (Onsite) Department: Manufacturing Reports to: Supervisor, Manufacturing About CTMC CTMC is a pioneering biotech joint venture, formed by National Resilience and MD Anderson Cancer Center, located in the heart of the Texas Medical Center. Our mission is to accelerate cell therapies from bench to bedside. We offer a wide range of cell therapy modalities, including CAR-T, TIL, and TCR-T. Our expert team collaborates closely with MD Anderson’s research and clinical faculty, bringing impactful cell therapies to cancer patients. Since inception in May 2022, our team has filed eight INDs and have received approval, without delay, demonstrating our commitment to delivering innovative treatments to patients with speed and precision. Our alliance with National Resilience enables us to remain at the forefront of biomanufacturing practices, leveraging advanced technology and processes to deliver exceptional results. Our growing, state-of-the-art, 60,000 sq. ft. industrial facility in the Texas Medical Center is staffed by an integrated team of industry veterans and academic scientists who are passionate about bringing life-saving cures to patients. Our unique joint venture structure, with two highly established partners, provides us with the financial stability and long-term horizon to achieve our organizational goals. At CTMC, we value our employees and offer a variety of development opportunities within our novel corporate structure to inspire professional growth and satisfaction. We foster a team-first culture and a balanced work-life environment to ensure our staff is energized and engaged in our mission to accelerate cell therapies from bench to bedside for patients who need them. If you share our passion for advancing the frontiers of medical science with innovative therapeutics and want to join a highly dedicated team committed to delivering novel cures to patients, we invite you to submit your application. We look forward to hearing from you and exploring how your skills and expertise can help us achieve our mission. Responsibilities Preparation of media and reagents from stock raw materials by maintaining aseptic technique during processing to ensure quality and integrity of cellular drug products. Execute media preparation master batch production records in a timely manner and maintain accurate documentation with FDA’s Good Manufacturing Practices. Provide support for routine maintenance activities, such as performing a daily, weekly, or monthly cleaning of the clean rooms when required. Perform routine or non-routine cleaning, kitting, documentation, processing, and materials procurement for the manufacturing department. Request and prepare materials for manufacturing operations in order to maintain proper inventory levels in the cleanroom at all times. Ensure transparent communication with staff, teams, support functions, and site leadership team. Other duties as required. Internship Development Opportunities : Observe various cell therapy modalities such as CAR-T, and TIL in GMP production. Exposure to GMP execution of cell therapy manufacturing processes such as primary cell culture, cell counting, isolation, transduction, expansion, harvesting, and cryopreservation. Observe and train on the following Cell Therapy equipment: CliniMacs Prodigies, G-Rexes, Incubators, BSC, Heat Sealers, NC-200 Cell Counter, Welders, and Lovos etc. Gain an understanding of current trends and technologies in the field of cell therapy. Experience working in a multidisciplinary team and developing communication skills. Qualifications/Skills High School Diploma required, enrollment in a minimum Bachelor’s degree program in a relevant field preferred, or enrollment in a specialized Cell Therapy or biotech degree program. Able to read and understand all applicable assigned standard operating procedures and policies. Able to understand and follow personnel flow, cleaning procedures, gowning requirements, and other protocols essential for maintaining cGMP-compliant operations within cleanroom facilities. Able to understand basic mathematical concepts. Able to work in a fast-paced environment. Demonstrated ability to be nimble, collaborative, and eager to contribute. Good communication skills. Proficient with MS Office (Excel, Outlook, etc.). Able to lift up to 40 lbs., work overhead and stand for extended periods of time. Working Conditions, Equipment, Physical Demands The incumbent in this position works in an office environment and cleanroom. The incumbent in this position will use the following equipment and shall have the following physical demands: Equipment- Computer, printer, telephone, and cleanroom equipment Physical Demands- Frequent standing, reaching, sitting and walking required Frequent lifting up to 10 lbs. required. Occasional lifting, pushing, and pulling up to 50 lbs. required. Frequent use of computer/keyboard required. The physical demands and work environment that have been described are representative of those an employee encounters while performing the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions in accordance with the Americans with Disabilities Act. The above job description is an overview of the functions and requirements for this position. This document is not intended to be an exhaustive list encompassing every duty and requirement of this position; your supervisor may assign other duties as considered necessary.

Keywords: CTMC, Sugar Land , Intern, Manufacturing, Science, Research & Development , Houston, Texas