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Clinical Laboratory Quality Coordinator

0-2 years
Not Disclosed
10 Sept. 26, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Clinical Laboratory Quality Coordinator

Category: Regulatory/Compliance
Location: Phoenix, Arizona, United States
Job ID: 2521151
Job Type: Full-Time
Remote: No (On-site)


Company Overview

LabCorp is seeking a Laboratory Quality Coordinator to join the CETWE team in Phoenix, AZ. The Quality Assurance team provides support to laboratories, senior management, clients, and other LabCorp sites. This role is ideal for laboratory professionals with a passion for quality and attention to detail.


Work Schedule

  • Monday – Friday: 8:00 AM – 4:30 PM

  • On-site position


Benefits

Employees working 20+ hours/week are eligible for:

  • Medical, Dental, Vision, Life insurance

  • Short-Term & Long-Term Disability (STD/LTD)

  • 401(k) with company match

  • Paid Time Off (PTO) or Flexible Time Off (FTO)

  • Tuition Reimbursement

  • Employee Stock Purchase Plan

Casual, PRN, & Part-Time employees (<20 hours/week): Eligible for 401(k) only.


Job Responsibilities

  • Support projects and activities related to quality assurance, control, improvement, and training

  • Prepare and support the laboratory for regulatory inspections

  • Maintain all necessary documents and materials required for inspections

  • Provide backup inspection support during inspections

  • Ensure compliance with proficiency testing and examinations

  • Coordinate and track external and internal proficiency testing

  • Perform internal audits and prepare audit reports

  • Prepare recurring quality reports for laboratory operations

  • Stay current with regulatory agency and proficiency test requirements

  • Initiate and manage Master Control forms for audit purposes

  • Participate in monthly Quality Meetings and compose minutes

  • Perform administrative and clerical duties as needed


Requirements

  • Associate’s degree or higher in Chemical/Biological Science, Clinical Laboratory Science, or Medical Technology

  • Previous experience as a Medical Technician or in a quality-related position

  • Prior clinical laboratory experience highly preferred

  • General knowledge of laboratory regulations (CAP/CLIA/ISO) and licensing requirements

  • Basic understanding of audit requirements and procedures

  • Working knowledge of quality assurance best practices and procedures

  • Excellent analytical, critical thinking, and problem-solving skills

  • Strong communication skills (written and verbal)

  • High attention to detail with strong organizational skills

  • Ability to work independently and within a team environment

  • Strong computer skills; proficient in MS Office programs


Equal Opportunity Employer Statement

LabCorp is committed to diversity, inclusion, and belonging. Employment decisions are based on qualifications and merit and are made without regard to:

  • Race, religion, color, national origin, sex, family/parental status, marital/civil union status

  • Sexual orientation, gender identity/expression, age, veteran status, disability, genetic information

  • Arrest or conviction records (considered in accordance with applicable law)

Applicants with disabilities who need assistance or accommodations can contact LabCorp Accessibility.

Privacy: See LabCorp Privacy Statement for details on data collection and storage.


How to Apply

If you are seeking a career with growth opportunities, professional challenges, and the ability to make a real impact, apply today!