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Qa Auditor -Trainer

2+ years
Not Disclosed
10 Nov. 12, 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: QA Auditor – Trainer

Category: Regulatory / Compliance
Location: Madison, Wisconsin, USA
Job ID: 2532296
Job Type: Full-Time
Remote: No


Company Overview

LabCorp is a leading global laboratory services company, providing critical support to research, clinical, and diagnostic laboratories. The Quality department ensures compliance with regulatory standards and supports continuous improvement across all operations.

  • Focus: Regulatory compliance, quality assurance, and training

  • Culture: Inclusive, diverse, and committed to equal opportunity employment


Role Overview

The QA Auditor – Trainer conducts quality audits, provides regulatory training, and ensures compliance within LabCorp’s research facilities. This role requires experience in a regulated environment, knowledge of LCMS, and the ability to train staff on quality standards.


Key Responsibilities

Quality Auditing & Compliance

  • Conduct work according to defined protocols and SOPs

  • Peer review QA SOPs and documentation

  • Ensure Regulatory Compliance and Quality Assurance (RC&QA) responsibilities are followed

  • Support ‘business partner’/liaison meetings representing QA function with operations

  • Report on quality metrics for assigned topics or departments and highlight trends

  • Adhere to required timelines for all assigned QA activities

Training & Support

  • Train staff on quality standards and regulatory requirements

  • Convey regulatory expectations clearly to operations teams


Qualifications & Requirements

Experience

  • Minimum 2 years in a regulated environment (GxP roles)

  • Experience in Bioanalysis (BioA) and/or LCMS

  • Knowledge of chromatography (HPLC), mass spectrometry/hybrid tandem MS, plate reading technologies (e.g., MesoScale, EliSpot, BioPlex)

  • Understanding of cell viability, cell potency testing, and flow cytometry principles

Education

  • Bachelor’s Degree in Life Sciences preferred (or equivalent experience)

  • Relevant experience may substitute for formal education

Skills & Knowledge

  • Ability to interpret and apply applicable regulations to monitor compliance

  • Ability to interpret data and identify quality-critical problems

  • Strong communication, presentation, and training skills


Benefits

Employees scheduled to work ≥20 hours/week are eligible for:

  • Medical, Dental, Vision, Life, STD/LTD coverage

  • 401(k) plan

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

  • Tuition Reimbursement

  • Employee Stock Purchase Plan

Casual, PRN, or part-time employees (<20 hours/week) are eligible for the 401(k) plan only.


Equal Opportunity Employer Statement

LabCorp is committed to inclusion and belonging and prohibits harassment or discrimination. Employment decisions are based on qualifications, merit, and business needs. Qualified applicants are considered regardless of:

  • Race, religion, color, national origin, sex, family/parental status, marital status, sexual orientation, gender identity/expression, appearance, age, veteran status, disability, genetic information, or other legally protected characteristics

  • Arrest or conviction records (considered per applicable law)

Accessibility: Individuals with disabilities needing assistance to search or apply online can contact LabCorp Accessibility.


How to Apply

  • Apply online via LabCorp careers site