Associate Director Clinical Quality Assurance Jobs in Texas
Associate Director Clinical Quality Assurance jobs in Texas are among the most active in the country, concentrated in pharmaceutical manufacturing, clinical research, biologics, and medical device sectors that have deep roots in the state. Houston, Dallas, and Austin are the primary hiring metros, with anchors like Johnson & Johnson, AbbVie, and Thermo Fisher Scientific maintaining significant Texas operations. Regulatory affairs oversight, GCP compliance, and inspection readiness are the most consistently sought specialties across postings. Find a role that fits below and apply directly.
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Showing 5 of 276+ Associate Director Clinical Quality Assurance jobs
The MD Anderson Cord Blood Bank Program creates a lifesaving product from something that was once considered medical waste. Umbilical cord blood is the blood that remains in the placenta and umbilical cord after a baby is born. This blood contains stem cells, which can be used to treat patients with many life-threatening diseases, including cancer. As a public cord blood bank, collectors collect voluntary donations from mothers at several Houston-area hospitals. Collecting cord blood poses no danger to either the mother or the baby. Our inventory is available to transplant facilities worldwide for patients who require stem cell transplantation.
SUMMARY
The Quality Assurance Specialist is responsible for managing the cleanroom facility and supporting all quality assurance operations, including document control, training, competency assessments, audits, and incident reporting. This role ensures compliance with the Cord Blood Bank Quality Assurance Program and regulatory/accreditation agencies such as the FDA, FACT, and CAP.
Key responsibilities include reviewing quality documentation, coordinating internal and external audits, reviewing batch and testing records, preparing CBUs for national and international registry listing, ensuring shipment readiness, and supporting continuous quality improvement.
At MD Anderson, we offer careers built on care, growth, and balance. Our employees enjoy a benefits package designed to support every stage of life, starting on day one.
- Paid employee medical benefits (zero premium) starting on first day for employees who work 30 or more hours per week
- Group Dental, Vision, Life, AD&D and Disability coverage
- Paid time off (PTO) and Extended Illness Bank (EIB) paid leave accruals
- Paid institutional holidays, wellness leave, childcare leave, and other paid leave programs
- Tuition Assistance Program after six months of service
- Teachers Retirement System defined-benefit pension plan and two voluntary retirement plans
- Employer paid life, AD&D and an illness-related reduced salary pay program
- Extensive wellness, recognition, fitness, employee health programs and employee resource groups
Key Functions
Environmental Monitoring & Facility Quality Compliance
- Oversee the Environmental Monitoring (EM) program, including sampling plans, routine trending, and excursion response procedures in alignment with regulatory guidelines and the CBB Quality Management Plan.
- Ensure EM is performed under static and dynamic conditions—including during product manufacturing—and that microbiological and particle data are trended and acted upon.
- Collaborate with MD Anderson's housekeeping team to ensure appropriate cleaning standards and staff competency for classified areas.
- Oversee qualification and quality control release testing for raw materials, in process materials, components, and final products, including growth promotion testing for all microbiology and EM media.
- Manage the automated monitoring system (daily/monthly review, alarm investigations, corrective actions, annual probe calibrations, and staff training).
- Maintain aseptic processing monitoring for both facility and personnel; drive corrective and preventive actions to maintain a controlled state.
- Review performance indicator data to identify, develop, and implement process improvements; manage environmental excursion investigations and ensure timely corrective actions.
- Develop, implement, and manage training and qualification of cleanroom staff (access, gowning, hygiene, aseptic technique, cleanroom behavior, and patient safety considerations).
- Ensure compliance with Employee and Environmental Health and Safety requirements.
- Collaborate with Institutional Facilities to ensure the cleanroom meets FDA Biological Licensure requirements.
- Perform quarterly safety inspections, communicate deficiencies, and ensure follow up is completed.
Quality Program Management
- Maintain up to date knowledge of technical procedures, policies, and regulations including FDA cGTP and cGMP, FACT NetCord, and CAP standards, and educate staff accordingly.
- Assist in developing and implementing training programs; identify improvement areas.
- Monitor staff training and competency; review and audit training records.
- Oversee the Proficiency Testing Program, submit final reports, investigate failures, and implement corrective actions.
- Mentor staff on SOP review and revision processes.
- Support the controlled document system including review, approval, implementation, revision, distribution, and archiving of documents.
- Perform annual review of assigned controlled documents and update as needed.
- Write, review, and revise technical SOPs and policies; ensure alignment with regulatory and accreditation changes.
- Design and execute validation studies and develop related SOPs and worksheets; ensure validation meets regulatory endpoints.
- Oversee qualification of assigned SOPs and mentor team members involved in these activities.
Quality System Support
- Conduct quality assurance reviews of third party lab results, manufacturing batch records, and quality control testing records (environmental monitoring, sterility, batch data, and CBU documentation). Ensure corrective actions are addressed and files are closed appropriately.
- Complete final CBU reviews for registry listing, confirming donor eligibility, licensure status, and conformance to BLA specifications.
- Review products for release, ensuring all criteria, investigations, and documentation—including Certificates of Conformance—are complete prior to clinical distribution.
- Review product testing, follow up on outstanding results, resolve reactive/abnormal findings, and report to physicians or agencies as appropriate.
- Inspect and release lot labels; investigate labeling errors or missing labels.
- Support the automated monitoring system (daily/monthly review, alarm investigations, corrective actions, probe calibration management, and staff training).
- Ensure proper documentation of deviations, incidents, out of specification results, product recalls, and complaints. Oversee staff training and competency monitoring.
- Perform quality management review of deviations/incidents, identify issues, support investigations, and determine corrective/preventive actions (CAPA). Track timely implementation.
- Support electronic submission of documentation for accreditation, licensing, and post marketing activities (clinical outcome data, changes, biological product deviations, adverse events, BLA, IND, CAP, FACT).
Other duties as assigned.
Education
Required: Bachelor's degree.
Preferred: Master's degree.
Experience
Required: Five years of relevant experience. With Master's degree, three years of required experience required.
Preferred: Experience with HCT/Ps in a quality control, quality assurance, or regulatory role. Experience manufacturing or testing clinical cellular therapy products. Experience in blood or tissue banking.
The University of Texas MD Anderson Cancer Center offers excellent benefits, including medical, dental, paid time off, retirement, tuition benefits, educational opportunities, and individual and team recognition.
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.
Additional Information
- Requisition ID: 181829
- Employment Status: Full-Time
- Employee Status: Regular
- Work Week: Day/Evening, Days, Evenings
- Minimum Salary: US Dollar (USD) 88,200
- Midpoint Salary: US Dollar (USD) 110,500
- Maximum Salary: US Dollar (USD) 132,300
- FLSA: exempt and not eligible for overtime pay
- Fund Type: Soft
- Work Location: Onsite
- Pivotal Position: No
- Referral Bonus Available?: No
- Relocation Assistance Available?: No
LI-Onsite
The MD Anderson Cord Blood Bank Program creates a lifesaving product from something that was once considered medical waste. Umbilical cord blood is the blood that remains in the placenta and umbilical cord after a baby is born. This blood contains stem cells, which can be used to treat patients with many life-threatening diseases, including cancer. As a public cord blood bank, collectors collect voluntary donations from mothers at several Houston-area hospitals. Collecting cord blood poses no danger to either the mother or the baby. Our inventory is available to transplant facilities worldwide for patients who require stem cell transplantation.
SUMMARY
The Quality Assurance Specialist is responsible for managing the cleanroom facility and supporting all quality assurance operations, including document control, training, competency assessments, audits, and incident reporting. This role ensures compliance with the Cord Blood Bank Quality Assurance Program and regulatory/accreditation agencies such as the FDA, FACT, and CAP.
Key responsibilities include reviewing quality documentation, coordinating internal and external audits, reviewing batch and testing records, preparing CBUs for national and international registry listing, ensuring shipment readiness, and supporting continuous quality improvement.
At MD Anderson, we offer careers built on care, growth, and balance. Our employees enjoy a benefits package designed to support every stage of life, starting on day one.
- Paid employee medical benefits (zero premium) starting on first day for employees who work 30 or more hours per week
- Group Dental, Vision, Life, AD&D and Disability coverage
- Paid time off (PTO) and Extended Illness Bank (EIB) paid leave accruals
- Paid institutional holidays, wellness leave, childcare leave, and other paid leave programs
- Tuition Assistance Program after six months of service
- Teachers Retirement System defined-benefit pension plan and two voluntary retirement plans
- Employer paid life, AD&D and an illness-related reduced salary pay program
- Extensive wellness, recognition, fitness, employee health programs and employee resource groups
Key Functions
Environmental Monitoring & Facility Quality Compliance
- Oversee the Environmental Monitoring (EM) program, including sampling plans, routine trending, and excursion response procedures in alignment with regulatory guidelines and the CBB Quality Management Plan.
- Ensure EM is performed under static and dynamic conditions—including during product manufacturing—and that microbiological and particle data are trended and acted upon.
- Collaborate with MD Anderson's housekeeping team to ensure appropriate cleaning standards and staff competency for classified areas.
- Oversee qualification and quality control release testing for raw materials, in process materials, components, and final products, including growth promotion testing for all microbiology and EM media.
- Manage the automated monitoring system (daily/monthly review, alarm investigations, corrective actions, annual probe calibrations, and staff training).
- Maintain aseptic processing monitoring for both facility and personnel; drive corrective and preventive actions to maintain a controlled state.
- Review performance indicator data to identify, develop, and implement process improvements; manage environmental excursion investigations and ensure timely corrective actions.
- Develop, implement, and manage training and qualification of cleanroom staff (access, gowning, hygiene, aseptic technique, cleanroom behavior, and patient safety considerations).
- Ensure compliance with Employee and Environmental Health and Safety requirements.
- Collaborate with Institutional Facilities to ensure the cleanroom meets FDA Biological Licensure requirements.
- Perform quarterly safety inspections, communicate deficiencies, and ensure follow up is completed.
Quality Program Management
- Maintain up to date knowledge of technical procedures, policies, and regulations including FDA cGTP and cGMP, FACT NetCord, and CAP standards, and educate staff accordingly.
- Assist in developing and implementing training programs; identify improvement areas.
- Monitor staff training and competency; review and audit training records.
- Oversee the Proficiency Testing Program, submit final reports, investigate failures, and implement corrective actions.
- Mentor staff on SOP review and revision processes.
- Support the controlled document system including review, approval, implementation, revision, distribution, and archiving of documents.
- Perform annual review of assigned controlled documents and update as needed.
- Write, review, and revise technical SOPs and policies; ensure alignment with regulatory and accreditation changes.
- Design and execute validation studies and develop related SOPs and worksheets; ensure validation meets regulatory endpoints.
- Oversee qualification of assigned SOPs and mentor team members involved in these activities.
Quality System Support
- Conduct quality assurance reviews of third party lab results, manufacturing batch records, and quality control testing records (environmental monitoring, sterility, batch data, and CBU documentation). Ensure corrective actions are addressed and files are closed appropriately.
- Complete final CBU reviews for registry listing, confirming donor eligibility, licensure status, and conformance to BLA specifications.
- Review products for release, ensuring all criteria, investigations, and documentation—including Certificates of Conformance—are complete prior to clinical distribution.
- Review product testing, follow up on outstanding results, resolve reactive/abnormal findings, and report to physicians or agencies as appropriate.
- Inspect and release lot labels; investigate labeling errors or missing labels.
- Support the automated monitoring system (daily/monthly review, alarm investigations, corrective actions, probe calibration management, and staff training).
- Ensure proper documentation of deviations, incidents, out of specification results, product recalls, and complaints. Oversee staff training and competency monitoring.
- Perform quality management review of deviations/incidents, identify issues, support investigations, and determine corrective/preventive actions (CAPA). Track timely implementation.
- Support electronic submission of documentation for accreditation, licensing, and post marketing activities (clinical outcome data, changes, biological product deviations, adverse events, BLA, IND, CAP, FACT).
Other duties as assigned.
Education
Required: Bachelor's degree.
Preferred: Master's degree.
Experience
Required: Five years of relevant experience. With Master's degree, three years of required experience required.
Preferred: Experience with HCT/Ps in a quality control, quality assurance, or regulatory role. Experience manufacturing or testing clinical cellular therapy products. Experience in blood or tissue banking.
The University of Texas MD Anderson Cancer Center offers excellent benefits, including medical, dental, paid time off, retirement, tuition benefits, educational opportunities, and individual and team recognition.
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.
Additional Information
- Requisition ID: 181829
- Employment Status: Full-Time
- Employee Status: Regular
- Work Week: Day/Evening, Days, Evenings
- Minimum Salary: US Dollar (USD) 88,200
- Midpoint Salary: US Dollar (USD) 110,500
- Maximum Salary: US Dollar (USD) 132,300
- FLSA: exempt and not eligible for overtime pay
- Fund Type: Soft
- Work Location: Onsite
- Pivotal Position: No
- Referral Bonus Available?: No
- Relocation Assistance Available?: No
LI-Onsite
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Where Texas roles are concentrated, by current openings.
Associate Director Clinical Quality Assurance Job Market in Texas
A snapshot from current Texas openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Technology & Software11
- Healthcare & Medical Services7
- Energy5
- Education5
- Aerospace & Defense5
What Texas Employers Look For
The qualifications that appear most often in associate director clinical quality assurance jobs across Texas.
- Bachelor's or advanced degree in life sciences, pharmacy, or a related field required
- Minimum seven to ten years of clinical quality assurance experience in pharma or biotech
- Deep working knowledge of FDA regulations, ICH guidelines, and GCP standards
- Proven experience leading quality audits, CAPA programs, and regulatory inspections
- Prior people management or cross-functional team leadership experience strongly preferred
- ASQ Certified Quality Auditor or RAC certification is a recognized differentiator in Texas
Associate Director Clinical Quality Assurance Jobs in Texas: Frequently Asked Questions
How do you become a associate director clinical quality assurance in Texas?
The path typically starts with a bachelor's degree in a life science, nursing, or pharmacy field, followed by progressive QA experience in clinical research or pharmaceutical manufacturing. Texas does not require a state-issued license specific to clinical QA, but many hiring managers expect credentials such as the ASQ Certified Quality Auditor or the Regulatory Affairs Certification. Candidates who build experience through CRO, biotech, or medical device roles in Texas hubs like Houston's Texas Medical Center or the DFW Metroplex tend to advance fastest.
Which companies hire associate director clinical quality assurances in Texas?
Texas associate director clinical quality assurance roles are posted by HEB, LMI, and DHL and others right now, based on current listings on Migrate Mate as of July 2026. Texas's dense concentration of pharma, biotech, and clinical research organizations across Houston, Dallas, and Austin keeps employer demand broad and consistent year-round.
Which Texas cities have the most associate director clinical quality assurance jobs?
Houston, Austin, and San Antonio have the most associate director clinical quality assurance openings in Texas. Houston leads because of the Texas Medical Center and its surrounding pharmaceutical and biotech corridor, while Dallas-Fort Worth attracts roles tied to large CROs, medical device firms, and corporate compliance functions, and Austin's growing life sciences and health tech sector drives demand there.
Are there remote associate director clinical quality assurance jobs in Texas?
Yes, and more than many QA roles, because the oversight, documentation review, and audit coordination responsibilities of this director-level position can transfer well to remote settings. About 24% of associate director clinical quality assurance openings tied to Texas are remote or hybrid as of July 2026, reflecting the desk-heavy nature of the role. Responsibilities tied to on-site inspection readiness or manufacturing floor oversight are the most likely to require in-person presence.
How can I get hired as a associate director clinical quality assurance in Texas with little or no experience?
The most realistic entry path is a QA specialist or clinical quality associate role within a Texas CRO, pharma company, or hospital network, then building toward the director level over several years. Large Texas employers like those based in the Texas Medical Center and the DFW biotech corridor regularly hire into QA coordinator and auditor roles that serve as the foundation. Earning an ASQ Certified Quality Auditor credential early and gaining hands-on CAPA and inspection experience accelerates advancement into associate director consideration.
Where can I find and apply to associate director clinical quality assurance jobs in Texas?
You can find and apply to associate director clinical quality assurance jobs in Texas on Migrate Mate, which lists current Texas openings from employers actively hiring right now. Search the available roles, find the ones that match your experience and preferred location within Texas, and apply directly to the ones that fit.
See All 276+ Associate Director Clinical Quality Assurance Jobs in Texas
Find roles in Texas that match your experience and apply in just a few clicks.
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