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Quest Diagnostics · Lewisville, TX · posted Jul 1, 2026

Manager, Quality Assurance

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The role

The Quality Assurance Manager directs the daily training, development, supervision, and scheduling of department personnel to ensure optimal operational efficiency and a continuous workflow. This role oversees core quality functions and works with other Quality Assurance staff to ensure the laboratory’s Quality Management System is followed but also provides input on how it can be evolved. The Quality Assurance Manager directly supports the Quality Assurance Director and CLIA Laboratory Director in maintaining the laboratory’s compliance with internal policies, regulatory standards, and company procedures.

Provides overall supervision to technical and administrative QA staff, managing talent selection, retention, onboarding, training, scheduling, performance evaluations, and counseling. The role directly supervises QA staff in the Specimen Management department. The role will monitor staff quality of service, deliver actionable feedback, and conduct comprehensive mid-year and annual performance reviews. Ensure efficient operation of the department to maximize employee utilization, maintain workflow continuity, and foster an environment of continuous improvement.

The role works with and supervises Quality Assurance staff in core quality functions, including tracking laboratory quality indicators; documenting and tracking of nonconformances; enrollment and adherence to proficiency testing requirements; execution of the laboratory’s internal audit program; maintaining the laboratory’s licensures and accreditations; adherence to public health reporting requirements; maintain client relationships; and others as necessary.

Prepare comprehensive reports for the Director of Quality Assurance and CLIA Laboratory Director, including Management Reviews. Assemble, maintain, and execute QA department standard operating procedures. Assist with offsite inspections as required. Performs other ancillary duties as assigned by leadership. Direct Reports: 3 Five years in a clinical laboratory setting A minimum of one year of supervisory experience Knowledge: Demonstrated knowledge in state and federal regulatory requirements for operating a clinical laboratory Knowledge of CAP accreditation and ISO15189 standards is desirable Skills: Demonstrated skills and training in Quality Improvement (e.g., Six Sigma, Lean, etc.) Proven track record in applying Quality Improvement methods Excellent communication skills, verbal and written Ability to work without direct supervision Demonstrated ability to lead a team Demonstrated ability to collaborate effectively across teams and functions Education: Bachelor's Degree Required MLS(ASCP) or equivalent laboratory professional license required ASQ (any) preferred

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