Quality Assurance Coordinator Job at Labcorp
Labcorp is seeking a Clinical Laboratory Quality Assurance Coordinator to support molecular and microbiology labs in Raritan, New Jersey. This QA Coordinator role is ideal for laboratory professionals with strong attention to detail, regulatory knowledge, and a passion for quality systems. As part of Labcorp’s Quality Assurance team, you will ensure regulatory readiness, support audits, maintain documentation, and uphold the highest standards of laboratory compliance. Join for the Clinical Laboratory Jobs at Labcorp, USA.
Job Details:
- Job Title: Clinical Laboratory QA Coordinator – Molecular & Microbiology
- Category: Regulatory/Compliance
- Location: Raritan, New Jersey, USA
- Job ID: 2535880
- Job Type: Full-Time
- Remote: No
- Pay Range: $29.00 – $33.00 per hour
- Work Schedule: Monday – Friday | 8:30 AM – 5:00 PM
- Benefits: Medical, Dental, Vision, Life, STD/LTD, 401(k), PTO/FTO, Tuition Reimbursement, Employee Stock Purchase Plan
About the Company:
Labcorp is a global leader in laboratory diagnostics and biotechnology solutions, delivering cutting-edge clinical insights that advance patient care. With a commitment to scientific excellence and quality, Labcorp supports healthcare providers and research institutions through innovative testing services and industry-leading laboratory operations. Also, the company offers various Life Science Research Jobs that uplift your career.
Educational Requirements for the QA Coordinator Role:
Bachelor’s degree in:
- Â Biological Science
- Clinical Laboratory Science
- Medical Technology
- OR a non-traditional bachelor’s degree meeting CLIA & state regulatory requirements
Key Responsibilities of the QA Coordinator:
- Support quality assurance, quality control, training, and improvement projects
- Prepare and maintain documentation for regulatory inspections
- Provide backup support during laboratory inspections
- Track proficiency testing (internal & external)
- Perform internal audits and prepare audit reports
- Prepare recurring quality reports for laboratory operations
- Stay updated on regulatory requirements (CAP/CLIA/ISO)
- Initiate and maintain Master Control forms for audits
- Participate in monthly Quality Meetings and write minutes
- Perform administrative and clerical duties as needed
Skills Required for the QA Coordinator Role:
- Minimum 1 year as a Technologist or QA-related role
- Clinical laboratory experience strongly preferred
- Microbiology and/or molecular experience preferred
- Knowledge of CAP/CLIA/ISO regulations
- Understanding of audit procedures and QA best practices
- Strong analytical, critical thinking, and problem-solving skills
- Excellent written and verbal communication
- High attention to detail and strong organizational skills
- Ability to work independently and in team settings
- Proficiency in MS Office and computer applications
How to Apply?
Create job alerts or apply directly through the Labcorp Careers portal to receive updates on similar QA, molecular, and microbiology roles.
