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Clinical Laboratory Quality Analyst

Labcorp
2+ years
Not Disclosed
Birmingham, United States
1 June 2, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes

Clinical Laboratory Quality Analyst

Category: Regulatory / Compliance
Location: Birmingham, Alabama, USA
Job ID: 2614622
Employment Type: Full-Time
Work Schedule: Monday – Friday, 8:00 AM – 5:00 PM (Onsite)


Job Summary

The Clinical Laboratory Quality Analyst supports the Quality Management System (QMS) by ensuring compliance with CAP, CLIA, ISO 15189, and other regulatory requirements. This role is responsible for quality data analysis, audit management, inspection readiness, regulatory compliance, corrective action support, and continuous quality improvement initiatives within the clinical laboratory environment.


Key Responsibilities

Quality Metrics & Reporting

  • Analyze monthly and quarterly quality metrics.

  • Generate and maintain quality performance reports.

  • Monitor quality trends and identify improvement opportunities.

  • Support metric tracking and reporting programs.

Quality Management System (QMS)

  • Support laboratory quality improvement initiatives.

  • Assist in maintaining and enhancing the regional laboratory Quality Management System.

  • Monitor and manage electronic quality systems including:

    • Competency management

    • Training management

    • Document control

    • Nonconforming event tracking

    • Quality metrics programs

Audits & Inspection Readiness

  • Schedule and conduct internal quality audits of laboratory departments and processes.

  • Prepare audit reports and communicate findings.

  • Assist in maintaining ongoing inspection readiness.

  • Support external audits and inspections conducted by:

    • CAP

    • CMS

    • ISO 15189

    • Other regulatory agencies

  • Participate in accreditation and regulatory inspections.

Regulatory Compliance

  • Stay updated on CAP, CLIA, ISO, and other regulatory requirements.

  • Serve as a compliance and regulatory resource for laboratory staff.

  • Assist with laboratory licensure and accreditation applications and renewals.

  • Support change control processes.

Quality Investigations & Corrective Actions

  • Assist in investigations of:

    • Nonconforming events

    • Quality incidents

    • Customer complaints

  • Facilitate:

    • Root Cause Analysis (RCA)

    • Corrective and Preventive Actions (CAPA)

    • Failure Mode and Effects Analysis (FMEA)

    • Risk Assessments

    • Effectiveness Checks

Training & Support

  • Train and educate staff on quality-related topics.

  • Provide guidance on quality standards, procedures, and compliance requirements.

  • Participate in monthly quality meetings and prepare meeting minutes.

Documentation & Systems Administration

  • Serve as site administrator for:

    • Document Control Systems

    • IQE Applications within MediaLab

  • Review proficiency testing results.

  • Maintain quality records and documentation.

  • Perform administrative and clerical support activities as required.


Minimum Qualifications

  • Associate’s Degree in:

    • Chemical Science

    • Biological Science

    • Clinical Laboratory Science

    • Medical Technology

  • 2+ years of clinical laboratory testing experience in a CLIA/CAP-accredited laboratory.


Preferred Qualifications

  • Bachelor’s Degree in:

    • Chemical Science

    • Biological Science

    • Clinical Laboratory Science

    • Medical Technology

  • 1+ year of quality assurance or quality management experience in a CLIA/CAP laboratory.