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Quality Manager

Job in Newport, Campbell County, Kentucky, 41072, USA
Listing for: Socket.dev
Full Time position
Listed on 2026-08-14
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
Salary/Wage Range or Industry Benchmark: 85000 - 120000 USD Yearly USD 85000.00 120000.00 YEAR
Job Description & How to Apply Below

Description

JOB OVERVIEW

The Quality Manager reports to the Laboratory Director and coordinates efforts that foster quality and ensure that all pre-analytical, analytical, and post-analytical processes are consistent with applicable state regulations, College of American Pathologist (CAP) standards, and the values and mission of Ethos Laboratories. This person is also responsible for collaborating with each department on quality initiatives and Proficiency Testing (PT) performance, as well as document control, licensing, and accreditation activities.

Finally, the Quality Manager completes the day-to-day activities of the quality department and serves as the primary point of contact for regulatory agencies.

ESSENTIAL FUNCTIONS

  • Manages Quality Department
  • Coordinates and maintains all quality assurance program activities
  • Maintains systems and controls to ensure consistency and compliance with applicable regulatory requirements
  • Collaborates with each department on the creation and monitoring of quality indicators for focused process, quality, or performance improvement
  • Plans for improved quality through the use of continuous quality improvement plans (cQIPs), blind audits, and focus studies as needed
  • Works with Laboratory Managers and Laboratory Director to ensure enrollment and participation in proficiency testing (PT) for each analyte, including review/submission of PT results, record keeping, identifying trends, reporting on PT performance in meetings, and maintaining spreadsheets
  • Maintains and updates (as needed) the Quality Management System (QMS)
  • Reviews, categorizes, interprets, and identifies trends with internal incident reports
  • Compiles and completes quarterly quality assessments and annual review of effectiveness
  • Holds quarterly Quality Committee meetings to discuss quality initiatives and performance
  • Participates in overall safety compliance initiatives and safety metrics per regulatory requirements; attends monthly Safety Committee meetings
  • Assumes other duties as assigned by the Laboratory Director
  • Supports the internal/external inspection process of the laboratory and associated sites to ensure compliance with applicable federal, state, and local regulations, College of American Pathologists (CAP) accreditation requirements, and Ethos standards
  • Serves as a resource regarding Clinical Laboratory Improvement Amendments (CLIA) regulations and CAP accreditation standards
  • Interprets regulations and standards for application in the laboratory and associated sites
  • Collaborates with department supervisors/managers in ensuring thorough understanding of and compliance with applicable regulations and standards
  • Coordinates pre-inspection meetings with CAP Team Leads as needed
  • Maintains current state and organizational licensing; coordinates submission of renewal documents as needed
  • Site Administrator for Media Lab software, including Document Control, Compass, and Inspection Proof
  • Maintains all controlled documents within Media Lab, assigning new document numbers and creating new manuals as needed
  • Ensures appropriate workflows for document review/approval process within Media Lab
  • Creates and supports the creation of continuing education materials within Media Lab
  • Maintains Inspection Proof within Media Lab to ensure the laboratory is inspection-ready at all times
  • Provides end-user training and/or troubleshooting as needed
  • Other duties as assigned

Requirements

PROFESSIONAL REQUIREMENTS

  • Understanding of and experience with high-complexity clinical laboratory operations
  • Analytical/critical thinking; able to analyze, interpret, and identify trends
  • Demonstrated success in collaborating and motivating team members to reach objectives
  • Ability to enact quality improvement through problem solving skills and knowledge of quality tools
  • Attitude focused on bringing solutions
  • Ability to properly manage, direct, and supervise a team
  • Proficient with Microsoft Office Applications

EDUCATION AND EXPERIENCE REQUIREMENTS

  • Bachelor’s degree (chemistry, physics, biology, clinical laboratory science, or medical technology) required
  • Minimum of three years of experience in a laboratory setting required
  • Preferred experience:

    Quality Assurance,…
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