Quality Assurance Manager

Quest Diagnostics Incorporated; Houston (TX); On-site; USD 105,000 - 150,000; Full time

Job summary

Quest Diagnostics Incorporated is seeking a Quality Assurance Manager in Houston, TX to lead and coordinate QA efforts across pre-analytical, analytical and post-analytical processes. The role ensures compliance with CAP accreditation, CLIA regulations, and state laws, while driving continuous improvement initiatives.

The position requires strong leadership, regulatory expertise, and the ability to manage proficiency testing, public health reporting, and quality metrics across the testing

Qualifications

• Bachelor of Science in Medical Technology, Biology or Chemistry is required.
• Masters in Biological Science or equivalent is preferred.
• CLIA '88 General Laboratory Supervisor qualifications are required.
• Foreign educated candidates must provide credential evaluation (IERF).
• US educated candidates must provide a detailed original transcript.

Responsibilities

• Lead and coordinate quality processes across pre-analytical, analytical and post-analytical stages.
• Ensure compliance with federal, state and local regulations and CAP accreditation standards.
• Oversee proficiency testing enrollment and corrective actions for non-conformances.
• Manage Public Health Reporting compliance across the region.
• Develop and monitor Quality Management System plans with actionable metrics.
• Address customer complaints and ensure timely revised reports where needed.

Skills

Quality Assurance leadership

Regulatory knowledge

Problem solving

Communication

Education

Bachelor of Science in Medical Technology, Biology or Chemistry

Master’s in Biological Science or equivalent (preferred)

General Laboratory Supervisor certification (CLIA '88)

IERF credential evaluation (foreign educated)

US transcript for US-educated candidates

Job description

The Quality Assurance Manager will lead, support, and coordinate efforts that foster quality and ensure that all pre-analytical, analytical and post-analytical processes are consistent with our company values and mission. Oversees Quality Assurance activities and ensures RRL Quality Assurance compliance.

This position is based in Houston, TX.

Responsibilities

Leadership

• Direct, advocate for and enable visibility of quality processes.
• Ensure accountability within all areas of the business unit (pre-analytical, analytical and post-analytical) such that every employee consistently exhibits behavior that promotes and supports quality.
• Influence may be exerted both directly and indirectly through the management of liaisons and intermediaries, such as department managers and supervisors as well as the Quality Assurance (QA) and Public Health Reporting staff.

Licensing and Accreditation

• Direct internal inspection process of the business unit, associated laboratories and specimen collection sites to ensure compliance with applicable federal, state, and local regulations, College of American Pathologists (CAP) accreditation requirements and Quest Diagnostics standards. Review and ensure that corrective action is implemented when non-conformances are found.
• Monitor published guidelines for revisions to regulations and/or accreditation standards and ensure laboratory compliance. Serve as a resource regarding Clinical Laboratory Improvement Amendments of 1988 (CLIA '88) regulations and CAP accreditation standards for all sites.
• Ensure all testing facilities/personnel have appropriate licensure and accreditation as deemed by federal, state, and local regulations. Collaborate with business unit management even if primary responsibility has not been assigned to QA.

Proficiency Testing

• Identify all tests performed and ensure enrollment and participation in external proficiency testing for each test. For those tests not covered by external proficiency testing, ensure internal proficiency testing is performed. Ensure that all proficiency testing is reviewed, and corrective action is complete for all non-conformances.

Public Health Reporting

• Ensure that the Public Health System is in compliance with Public Health Reporting Laws of all the states within the region.
• Manages the Public Health functions of the staff.

Quality Assurance/Quality Improvement

• Ensure that a defined instrument-to-instrument, method-to-method, and laboratory-to-laboratory comparison process, with fixed criteria for accessing acceptability, is performed and documented at least semi-annually.
• Conduct monthly QA meetings with required participation by all areas (including RRLs) having an impact on pre-analytical, analytical and post-analytical phases of testing (exception Billing).
• Ensure that each department has a comprehensive Quality Management System plan with monitors and that each department communicates their metrics and implements appropriate actions.
• Develop, monitor and improve Quality Assurance specific quality indicators, including but not limited to: Reportable Quality Issues, Proficiency Testing outcomes, Revised Reports tracking, and performance on inspections.
• Ensure all applicable employees are trained and comply with local quality policies. Ensure all QA policies have a biennial review.
• Ensure a process is in place to resolve customer complaints regarding pre-analytical, analytical, and post- analytical issues.
• Ensure performance of required Corporate Quality Inspection Program, Patient Results Distribution Program, Life Cycle Management Team Initiative/Database Changes Verification Program and other monitoring programs specifically assigned by Medical Operations and Quality (MOQ).
• Ensure enrollment and participation in external federal and state cytology proficiency testing as well as required educational programs.

Quality Control

• Act as a contact for national Quality Control (QC) peer comparison programs and ensure enrollment and effective corrective action as appropriate.

Quality Assurance Initiatives

• Ensure all duties are appropriately delegated as required by applicable federal, state and local regulations.
• Ensure that all departments have a process to identify and evaluate the relationship of patient information to patient test results. Ensure the process is in place, up to date, distributed and that all personnel are in compliance.
• Ensure prompt and complete reporting Reportable Quality Issues in compliance with the Standard Operating Procedure (SOP) and ensure effective corrective action including issuance of revised reports as applicable.
• Ensure complete tracking of revised reports in compliance with the SOP and ensure effective corrective action.
• Ensure compliance with all Quest standards as required.

Qualifications

• Bachelor of Science in Medical Technology, Biology or Chemistry.
• Masters in Biological Science, or equivalent, is preferred.
• Certifications and qualifications, as General Laboratory Supervisor, as defined by CLIA '88 are required.
• Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation).
• United States educated candidates must provide a detailed original transcript.

Work Experience

• Minimum of six years clinical experience with two years participating in Quality Assurance initiatives or QA leadership roles.
• Direct or Indirect people leader experience is preferred.

Other

• Must demonstrate effective communication and collaboration skills within department as well as with other functions within the company and third parties (ie., clients).
• Must have the ability to establish work priorities for self and others and handle several procedures simultaneously.
• Demonstrated success in motivating team members to reach objectives is highly desirable.
• Ability to schedule and manage resources to meet department goals.
• Must protect patient confidentiality at all times.

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