JOB DETAILS

Quality Assurance Specialist III

CompanyTexas Biomedical Research Institute
LocationSan Antonio
Work ModeOn Site
PostedJune 8, 2026
About The Company
Texas Biomedical Research Institute (Texas Biomed) is one of the world's leading independent biomedical research institutions dedicated to advancing health worldwide through innovative biomedical research. Texas Biomed, formerly the Southwest Foundation for Biomedical Research, partners with hundreds of researchers and institutions around the world, targeting advances in the fight against cardiovascular disease, psychiatric disorders, Tuberculosis, AIDS, hepatitis, malaria, parasitic infections, Ebolavirus, Marburg virus and a host of other infectious diseases. The Institute is located on a 200-acre campus on the northwest side of San Antonio, Texas. Its staff of more than 300 employees includes a multidisciplinary team of doctoral-level scientists who lead more than 200 major research projects in the Institute's Scientific Programs; Host-Pathogen Interactions, Disease Intervention & Prevention and Population Health. Texas Biomed is the site of the Southwest National Primate Research Center and the world's largest colony of baboons for biomedical research, including a unique pedigreed colony of approximately 2,500 nonhuman primates. The Institute enjoys a distinguished history in the innovative, humane and appropriate use of nonhuman primates for biomedical research. The Institute also is home to the nation's only privately-owned biosafety level 4 (BSL-4) laboratory. This maximum containment lab allows for safe research on lethal pathogens for which there are no treatments or vaccines, including potential bio-terror agents and emerging diseases. The AT&T Genomics Computing Center houses the world's largest computer cluster for human genetic and genomic research. This high-performance computing facility allows scientists to search for disease-influencing genes at record speed. For more information on Texas Biomed, visit us at www.TxBiomed.org
About the Role

Description

Join our growing Quality team as a Quality Assurance Specialist III.  This role will provide audit and regulatory compliance support for preclinical and animal studies.


THE ROLE:

• Perform audits for GLP preclinical and Animal Rule Studies as assigned and assure that the facilities, equipment, personnel, methods, practices, records and controls are compliant with applicable federal regulations and Texas Biomed internal standards.

• Complete facility-based, process-based, and study-specific audits; audit study protocols, data and records, and reports following written QAU SOPs, policies and directives.

• Maintain copies of the Master Schedule of GLP Studies and Animal Rule Studies and all GLP and Animal Rule protocols regarding studies assigned.

• Provide support for nonclinical/preclinical research studies including Quality review of data and reports and recommend corrective actions to study directors/principal investigators and/or study staff

• Perform Quality Assurance review of SOPs and associated forms for consistency, clarity and adherence to FDA GLP and Animal Rule regulations, and other regulatory standards for Texas Biomed.

• Independently collaborate with specific functional groups providing guidance on SOPs (i.e. content, quality, SOP lifecycle) and address any documentation needs.

• Provide support during regulatory inspections and internal functional group audits. Solid understanding of documents governing the inspection readiness.

• Assist with management of employee training documentation to ensure that Texas Biomedical Research Institute employee training files contain current and complete training information to ensure regulatory compliance.

• Assist in preparing materials for training programs and meetings.


OUR IDEAL CANDIDATE:

• Bachelor’s degree in science, biochemistry, biology or related field from an accredited college/university required. 

• Minimum of Three (3) years of job-related experience required. 

• Experience with Good Laboratory Practice standards and experience working in a GLP regulated research environment. 

• Experience in QA or QC, with focus on bioanalytical laboratory assays.

• RQAP-GLP Registration preferred.

• Specialized skills in Quality related work .

• Specialized skills that may be technical or non-technical, such as research and analytical skills, composing non-routine documents and letters, and ability to use software in complex applications.

• Understand regulations governing the conduct of nonclinical/preclinical research protocols.

• Understand medical and scientific terminology.


WHAT WE CAN OFFER YOU: 

• Enjoy an employee-centered culture grounded in open communication, empowerment, and trust. We believe in working hard and having fun, offering 100+ culture events each year to bring our team together and keep the energy strong!

• Comprehensive health, dental, vision, and life insurance coverage for you and your family—including pet insurance options.

• Competitive employer-funded retirement plan with 6% contributions starting on day one, increasing with years of service.

• Generous paid time off, including 14 paid holidays and a paid Winter Recess (from the last week of December through New Year’s).

• Paid time off for short-term illness and mental wellness, helping you take the time you need when life happens.

• Volunteer Time Off (VTO) to encourage giving back to the community.

• Paid parental leave to support you and your growing family.

• Flexible work arrangements that support a strong work-life balance.

• On-site medical clinic, wellness incentives, and prescription support programs designed to make care more accessible and affordable.

• On-site fitness center and wellness programs to help you stay active and healthy.

• Relaxed dress code so you can feel comfortable and be yourself at work.

• Dynamic learning environment with professional development opportunities, mentorship, tuition reimbursement, and leadership programs to support your growth.

• Proud recipient of the 2025 Healthy Workplace Platinum Recognition from the San Antonio Business Group on Health (SABGH)—the highest honor for employee-focused wellness initiatives.


WHO WE ARE: 

• Texas Biomedical Research Institute is one of the world's leading independent biomedical research institutions dedicated to advancing global human health through innovative biomedical research. Texas Biomed aims to unravel the mysteries of infectious diseases through innovative thinking, creative problem solving and cutting-edge technologies. 

• Texas Biomed is the only independent, nonprofit infectious disease research institute in the U.S. to combine: 

• The highest-level biocontainment labs for infectious disease and biodefense research

• A federally-designated National Primate Research Center 

• More than 80 years of discoveries advancing diagnostics, vaccines and therapies

• An entrepreneurial culture and specialized expertise in regulated science required for FDA approval


We take pride in fostering a culture of respect, opportunity, and unity! Texas Biomedical Research Institute provides equal employment opportunities for all qualified employees and applicants without regard to race, color, sex, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status.



Key Skills
GLP AuditingRegulatory ComplianceQuality AssuranceQuality ControlBioanalytical Laboratory AssaysSOP ReviewData ReviewAudit ManagementTechnical WritingAnalytical SkillsResearch SkillsRegulatory Inspection Support
Categories
Science & ResearchHealthcareEngineering
Benefits
Health InsuranceDental InsuranceVision InsuranceLife InsurancePet InsuranceRetirement PlanPaid Time OffPaid HolidaysWinter RecessSick LeaveMental Wellness LeaveVolunteer Time OffPaid Parental LeaveFlexible Work ArrangementsOn-site Medical ClinicWellness IncentivesPrescription Support ProgramsOn-site Fitness CenterRelaxed Dress CodeProfessional DevelopmentMentorshipTuition ReimbursementLeadership Programs
Job Information
📋Core Responsibilities
Perform audits for GLP preclinical and Animal Rule studies to ensure compliance with federal regulations and internal standards. Provide quality review of data, reports, and SOPs while supporting regulatory inspections and employee training documentation.
📋Job Type
full time
📊Experience Level
2-5
💼Company Size
434
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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