Quality Assurance - AP/CP Mgr- Irving, TX req37019 in Irving, TX at Quest Diagnostics

Date Posted: 2/12/2020

Job Snapshot

Job Description

Quality Assurance - AP/CP Mgr- Irving, Texas - 

Look for more than answers. Patients and Physicians rely on our diagnostic testing, information and services to help them make better healthcare decisions. These are often serious decisions with far reaching consequences, and require sensitivity, tact and a clear dedication to service. It’s about providing clarity and hope. 

You will work for the world leader in the industry, with a career where you can
expand your skills and knowledge. You’ll have a role where you can act with
professionalism, you can inspire colleagues, and you can care about the work we do and the people we serve. 

At Quest, we are on a continuous journey of discovery and development. It’s this attitude that has made us an industry leader and the #1 Diagnostic Lab in the US. For those joining us, we offer exciting and fast moving career opportunities where you can affect change at a rate unheard of in many organizations of our size and scope. While we invest in and develop technology to drive our innovations, our ongoing success relies on our people.


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.



  • 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 supervisiors as well as members of the Quality Assurance (QA) Committee.

  • Direct, advocate for and enable visibility of quality processes.  Ensure accountability within the Rapid Response Laboratories (RRLs) and Metro Laboratories 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 Medical Directors, managers or supervisors.

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.

  • Ensure that a Validity Check program is in place, as well as a Blind Samples resubmission program, if applicable.

  • 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.

Quality Assurance/Quality Improvement

  • Conduct monthly QA meetings with required participation by all areas (including RRLs and Metro Laboratories) having an impact on pre-analytical, analytical and post-analytical phases of testing (exception Billing).  Create effective materials (e.g., graphs, charts) to promote Quality Improvement (QI) and present plans and results at monthly meetings.

  • Ensure that each department has a comprehensive Quality Improvement 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.

  • Prepare, revise and distribute a QA Manual that includes local QA policies.  Ensure all applicable employees are trained and comply with policies.  Ensure all QA policies have annual 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 Surveillance Program, Patient Results Distribution Program, Best Practice Team Initiative/Database Changes Verification Program and other monitoring programs specifically assigned by National Quality Assurance (NQA).

  • 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 of 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 NQA standards as required.



Bachelor's degree (chemical, physical, biological or clinical laboratory science or medical technology)--required


  • Qualification as General Laboratory Supervisor as defined by CLIA ’88--desirable

  • Certification by American Society of Clinical Pathologists (ASCP)(or equivalent)--desirable

  • Certification by American Society for Quality (ASQ)--desirable

  • Six Sigma Green Belt Training--desirable

Work Experience

  • At least eight years employment in a laboratory setting with at least four years of direct supervisory experience in the clinical or anatomical pathology laboratory--required

  • Experience with Quality Assurance, statistical Quality Control, and laboratory regulations/accreditation requirements--required

  • Experience with managing complex programs with accountability for measured outcomes--required


  • Demonstrated ability to influence and create change--required

  • Strong interpersonal communication skills--required

  • Demonstrated strong writing and composition skills--required

  • Demonstrated success in motivating team members to reach objectives--desirable

  • Strong influencing skills--desirable

Business Process Skills

  • Understands clinical laboratory operations--required

  • Able to effect Quality Improvement through problem solving skills and knowledge of quality tools--required

  • Able to manage change--required

  • Organization skills--required

  • Project management skills--required

  • Analytical skills--required

  • Technical skills--required

  • Computer skills--required

  • Able to function in a matrix organization--desirable

  • Multi-tasking skills--desirable

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