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MD Anderson’s Molecular Diagnostic Laboratory seeks a Clinical Laboratory Supervisor to lead daily testing operations, ensure quality and regulatory compliance, and mentor a technical team. You will oversee SOP updates, evaluate new methods and instrumentation, and contribute to LIS/EMR implementations, focusing on accurate diagnoses and exceptional cancer care.
Join a world-leading cancer center and drive continuous improvement, staff development, and operational excellence across all testing
Join MD Anderson’s Molecular Diagnostic Laboratory as a Clinical Laboratory Supervisor and help lead the specialized testing operations that support accurate diagnoses and exceptional cancer care. You’ll combine technical expertise with hands‑on leadership to oversee daily laboratory activities, maintain rigorous quality standards, and guide a team responsible for delivering reliable clinical testing at one of the world’s leading cancer centers.
What’s in it for you? This is an opportunity to take ownership of laboratory operations while serving as a technical resource and people leader. You’ll supervise daily workflows, troubleshoot complex testing and computer‑related challenges, maintain and update standard operating procedures, and lead the evaluation and validation of new methodologies, tests, and instrumentation. You’ll also contribute to laboratory information system (LIS) and electronic medical record (EMR) implementations, helping ensure systems and processes support efficient, high‑quality testing.
You’ll have a direct impact on team performance, professional development, and laboratory culture. From onboarding and training employees to conducting competency assessments, coaching staff, managing schedules, and addressing performance concerns, you’ll help build a cohesive team focused on communication, accountability, and excellence. You’ll also identify and lead process improvements that strengthen productivity and laboratory operations while ensuring every phase of testing—from pre‑analytical through post‑analytical is performed according to established procedures.
Quality and regulatory compliance are central to this role. You’ll oversee quality control, quality assurance, and quality improvement activities; support compliance with regulatory and accreditation requirements; coordinate proficiency testing in accordance with CAP standards; and participate in mock inspections and other quality surveillance activities. You’ll also help evaluate new tests and processes through test cost analysis, business planning, training, and implementation, while ensuring laboratory supplies and equipment are available to meet operational needs. MD Anderson offers competitive pay, an annual merit increase program, annual incentive opportunities, an employer‑funded pension contribution, medical, dental and vision coverage, generous paid time off, and opportunities for professional growth and development.
Bring your technical knowledge, problem‑solving abilities, and commitment to developing people to a leadership role where you can strengthen laboratory performance and help advance the quality of cancer diagnostics at MD Anderson.
Other duties as assigned
Required: Bachelor’s Degree in a related science field or Molecular Genetic Technology++OR++Successful completion of a National Accrediting Agency for Clinical Laboratory Science (NAACLS) accredited Clinical Laboratory Science/Molecular Genetic Technology accredited program
Preferred: Master’s Degree in a related science field Doctorate in a related science field
Required: 8 years of clinical laboratory compliance and operations experience to include three years of lead or supervisory experience ++OR++ 6 years of clinical laboratory compliance and operations experience to include three years of lead or supervisory experience, with Master’s degree ++OR++ 4 years of clinical laboratory compliance and operations experience to include three years of lead or supervisory experience, with Doctorate degree
Successful completion of the LEADing Self Accelerate and/or LEADing Self Discover programs may substitute for one year of required supervisory or management experience. Completion of both programs can be substituted for a maximum of two years of supervisory or management experience.
2 years of clinical laboratory compliance and operations experience may be substituted for required certification.
Required (upon hire): ASCP — American Society of Clinical Pathologist Technologist/Scientist/Specialist certification OR CHS — Certified Histocompatibility Specialist, American Society for Histocompatibility and Immunogenetics (ACHI) OR CHT — Certified Histocompatibility Technologist, American Society for Histocompatibility and Immunogenetics (ACHI) OR MDT — Molecular Diagnostics Tech, American Medical Technologists (AMT) OR MT — Medical Technologist, American Medical Technologists (AMT)
Must pass pre-employment skills test as required and administered by Human Resources.
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. http://www.mdanderson.org/about-us/legal-and-policy/legal-statements/eeo-affirmative-action.html