Clinical Laboratory Quality Analyst

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives. Labcorp is seeking a Quality Assurance Analyst to join our team in Dublin, OH . Work Schedule: Monday - Friday 8:00am - 5:00pm Job Responsibilities Maintain and support the laboratory Quality Management System (QMS) in accordance with CLIA, CAP, ISO 15189, and other regulatory standards Monitor compliance with policies, procedures, and regulatory requirements Assist with internal and external audits, inspections, and accreditation activities Track and trend nonconformances, deviations, and corrective actions (CAPA) Collect, analyze, and interpret laboratory quality data (e.g., QC, proficiency testing, turnaround time, specimen rejection rates) Identify trends, shifts, or outliers using statistical tools Develop dashboards and reports to communicate quality performance metrics Perform root cause analysis and support data-driven decision making Partner with laboratory leadership and technical staff to implement continuous improvement initiatives Evaluate workflow efficiency and recommend process optimization strategies Support Lean, Six Sigma, or similar initiatives where applicable Apply knowledge of pre-analytical, analytical, and post-analytical processes Collaborate with technical teams to investigate quality issues and instrument or assay-related trends Assist with validation/verification studies, including stability, precision, and method comparisons Maintain quality documentation including SOPs, policies, and records Ensure proper documentation for audits and inspections Provide training or guidance on quality processes and data interpretation Keep up with all required proficiency testing and examinations Coordinate and track external and internal proficiency testing Participate in monthly Quality Meeting and compose minutes Minimum Qualifications Associate’s degree in a Chemical or Biological science, Clinical Laboratory Science or Medical Technology 2 years or more of clinical laboratory testing experience Preferred Qualifications Bachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science or Medical Technology 1 year or more of data analysis experience 1 year or more of quality experience in a clinical laboratory  Additional Job Standards In lieu of education requirements listed above, non-traditional degrees with applicable science credits that meet CLIA standards may meet education requirements Familiarity with an electronic data management system is a plus (i.e. MasterControl) General knowledge of laboratory regulations (CAP/CLIA/ISO) and licensing requirements Understanding of laboratory operations as well as policies and procedures Experience working in a high volume laboratory environment Basic understanding of audit related requirements and procedures Working knowledge of quality assurance best practices and procedures Excellent analytical, critical thinking and problem solving skills Ability to work independently and within a team environment Proficient with computers; Familiarity with laboratory information systems High level of attention to detail along with strong communication and organizational