Job Title: Clinical Laboratory Quality Analyst / Point of Care Coordinator
Category: Regulatory/Compliance
Location: Wichita, Kansas, United States
Job ID: 2522110
Job Type: Full-Time
Remote: No
Company Overview
LabCorp is seeking a Clinical Laboratory Quality Analyst / Point of Care Coordinator to join the team in Wichita, KS. The Quality Assurance team provides support to laboratories and senior management, ensuring quality results, regulatory compliance, and improved patient/provider satisfaction. This role manages point of care instruments, testing competencies, quality control, and reagent/supply management for bedside testing units.
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
Provide data and support for quality improvement initiatives
Schedule, conduct, and report on QA audits and inspections
Ensure readiness for inspections and maintain required documentation
Participate in regulatory and accrediting agency inspections
Draft responses to regulatory complaints and inspections
Stay current with regulatory and proficiency testing requirements
Participate in monthly Quality Meetings and compose minutes
Serve as a resource for regulatory compliance and point of care (POC) testing
Manage POC instruments, reagents, QC materials, and competencies
Monitor middleware for barcode scanning, testing, and resulting errors
Oversee analyzer/cartridge failures and coordinate service or replacements
Develop and validate new POC test setups, including project management and policy authorship
Provide administrative, technical, and educational guidance on POC testing
Ensure compliance with all regulatory and accreditation standards for safety and POC testing
Review, analyze, and report POC quality control and compliance data
Provide guidance and leadership for POC functions across multiple departments
Requirements
Bachelor’s degree in Chemical/Biological Science, Clinical Laboratory Science, or Medical Technology
2+ years experience as a Medical Technologist in a core lab setting
Prior experience in a quality-related role preferred
Familiarity with electronic data management systems (e.g., MasterControl) is a plus
General knowledge of laboratory regulations (TJC/CLIA/FDA/FACT) and licensing requirements
ASCP certification preferred
Strong understanding of audit requirements and quality assurance/management best practices
Excellent analytical, critical thinking, and problem-solving skills
Strong written and verbal communication skills
High attention to detail with strong organizational skills
Ability to work independently and in 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 that offers growth opportunities, professional challenges, and the chance to make a real difference, apply today!
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