Intern, Quality Assurance Document Control
Company: CTMC
Location: Houston
Posted on: February 15, 2026
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Job Description:
Job Description Job Description Location: Houston, TX (Onsite)
Department: Quality Assurance Reports to: Associate Director,
Compliance and Quality System 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 Process controlled
document requests, including creation, revision, approval,
issuance, and archival. Issuance of controlled documents for
manufacturing operations. Receive, review, and log incoming
documentation (SOPs, batch records, protocols, specifications)
Check in/out controlled documents, ensuring proper version control,
and revision history. Scan and archive hardcopy documents into the
electronic document management system. Maintain filing systems for
physical records, including off-site archives. Perform routine
checks on document repositories to identify missing or misfiled
records. Maintain document logs, indices, and archival storage
systems. Maintain the integrity of the Document Management System
(paper-based). Control access and distribution of documents to
authorized personnel only. Ensure documents are formatted according
to company standards and comply with cGMP requirements. Provide
basic troubleshooting and user support for document management
software. Other duties as assigned. 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. Previous
laboratory experience preferred. Able to learn testing procedures
and work utilizing standard operating procedures. 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.). Working
Conditions, Equipment, Physical Demands The incumbent in this
position works in an office environment. The incumbent in this
position will use the following equipment and shall have the
following physical demands: Equipment- Computer, printer, fax,
telephone, and laboratory testing equipment Physical Demands-
Occasional standing and walking required Frequent sitting,
reaching, and computer/keyboard usage Occasional lifting, pushing,
and pulling up to 10lbs.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, The Woodlands , Intern, Quality Assurance Document Control, Administration, Clerical , Houston, Texas