Job Description
Lead Laboratory Quality
Lead, support and coordinate efforts that foster and establish laboratory quality and ensure that all pre-analytical, analytical and post-analytical processes are consistent with our company values and mission.
This is a Hybrid position (3 days onsite, 2 days Work from Home)
Pay Range: $93,000 - $140,000/ year
Salary offers are based on a wide range of factors including relevant skills, training, experience, education, and, where applicable, certifications obtained. Market and organizational factors are also considered. Successful candidates may be eligible to receive annual performance bonus compensation.
We are proud to offer best-in-class benefits and programs to support employees and their families in living healthy, happy lives. Our pay and benefit plans have been designed to promote employee health in all respects – physical, financial, and developmental. Depending on whether it is a part-time or full-time position, some of the benefits offered may include:
- Medical/Prescription Drugs
- Dental
- Vision
- Flexible Spending Accounts (FSAs)
- Supplemental Health Plans
- 401(k) Plan – Company match dollar-for-dollar up to 5%
- Employee Stock Purchase Plan (ESPP)
- Supplemental Life Insurance
- Dependent Life Insurance
- Short- and Long-Term Disability buy-up
- Blueprint for Wellness
- Emotional Well-Being Resources
- Educational Assistance
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 supervisors and members of the Quality Assurance (QA) Committee.
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 and Laboratory Instrumentation Validation
- 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
Quality Management
- Conduct monthly QA meetings with required participation by all areas having an impact on pre-analytical, analytical and post-analytical phases of testing. 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 or Plan that includes local QA policies. Ensure all applicable employees are trained and comply with policies. Ensure all QA policies have annual review as required.
- 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). Quality Control
- Act as a contact for national Quality Control (QC) peer comparison programs and ensure enrollment and effective corrective action as appropriate.
- 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 and other key metrics are in compliance with the SOP and ensure effective corrective action when necessary.
- Ensure compliance with all Quest MOQ/CAP, and CLIA standards as they apply to the lab operations.
Qualifications
Required Work Experience:
6 + years of experience in the laboratory including people management and quality assurance duties.
Preferred Work Experience:
6 + years of experience in the laboratory including people management and 4 + years of direct responsibility for quality assurance, and/or quality control and/or quality program management
Physical and Mental Requirements:
- Ability to sit for up to 8 hours working at a desk
- Ability to lift 15 or more pounds
- Ability to travel, via automobile and aircraft
Knowledge:
Laboratory Operations, Quality Operations, Regulations (i.e., CAP, CLIA)
Skills:
- Proficiency in computer operations and Microsoft suit of applications
- Team management
- Negotiation and influence as a leader
- Problem solving and use of knowledge and logic to resolve complex issues
Education
- Bachelor's Degree in a chemical, physical, biological, clinical laboratory science or medical technology program (Required)
Licenses and Certifications
- MT ASCP certification is required (or similar).
- ASQ certification (preferred)
- Certifications Qualification as General Laboratory Supervisor as defined by CLIA '88 (preferred)
About the Team
Quest Diagnostics honors our service members and encourages veterans to apply. While we appreciate and value our staffing partners, we do not accept unsolicited resumes from agencies. Quest will not be responsible for paying agency fees for any individual as to whom an agency has sent an unsolicited resume. Equal Opportunity Employer: Race/Color/Sex/Sexual Orientation/Gender Identity/Religion/National Origin/Disability/Vets or any other legally protected status.
Job Info
- Job Identification 61490
- Job Category Quality Assurance
- Posting Date 06/10/2026, 05:35 PM
- Job Schedule Full time
- Job Shift Day
- Locations 1737 Airport Way S, Seattle, WA, 98134, US
- Workplace On-site 3 days/week
- Regular or Temporary Regular
- Weekly Working Hours 40.00
- Salary Minimum 93,000.00
- Salary Maximum 140,000.00
- AIP Target % 10
Job Tags
Full time, Temporary work, Part time, Work experience placement, Local area, Flexible hours, Shift work, 3 days per week