Clinical Laboratory Quality Analyst - Core Laboratory

Labcorp • Raritan, NJ

103d • $75,000 - $90,000

About The Position

LabCorp is seeking a Laboratory Quality Analyst to join our team in Raritan, NJ. The Quality Assurance team provides vital support to the laboratories, senior management, as well as our clients and other LabCorp sites. The Quality Analyst will be responsible for supporting projects and activities related to quality assurance, quality improvement, quality training, and other responsibilities of the Quality Assurance department. The Quality Analyst allows the laboratory to provide quality results to our providers and patients, which increases customer satisfaction and solidifies loyalty for our company.

Requirements

• Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology, or a non-traditional Bachelor's degree that meets local regulatory (CLIA & State) requirements
• 5 years of previous experience as a Technologist or in a quality-related position in a clinical laboratory is required
• Familiarity with an electronic data management system is a plus (i.e. MasterControl)
• General knowledge of laboratory regulations (CAP/CLIA/ISO) and licensing requirements
• Strong understanding of audit-related requirements and procedures
• Working knowledge of quality assurance/quality management best practices, pertaining to the clinical laboratory
• Excellent analytical, critical thinking, and problem-solving skills
• Strong communication skills; both written and verbal
• High level of attention to detail with strong organizational skills
• Ability to work independently and within a team environment
• Strong computer skills with proficiency with MS Office programs

Responsibilities

• Provide monthly and quarterly quality metric reports for clients and leadership using databases and crystal reports
• Assist staff with training in MasterControl, update and maintain all lab general and quality procedures, forms, and associated documents
• Provide data for quality teams and support all Quality Improvement efforts
• Schedule and conduct QA audits and inspections of assigned departments/facilities and perform audit reports
• Ensure complete and accurate readiness for all inspections and maintain all necessary documents
• Participate in regulatory and accrediting agency inspections when needed
• Perform first-level review of proficiency testing results, as well as monthly monitoring of QC data for all instrumentation within the department
• Assist with method/test validations, including data organization and performing initial review of all validation studies prior to review by the medical and/or technical director
• Draft responses to regulatory complaints and the results of inspections
• Stay current with all regulatory guidelines and proficiency test requirements
• Monitor the progress of implementation and subsequent use of electronic document management systems
• Participate in monthly Quality meetings and compose minutes
• Serve as a resource on regulatory issues, compliance, and quality management
• Perform administrative and clerical duties as needed

Benefits

• Medical
• Dental
• Vision
• Life
• STD/LTD
• 401(k)
• Paid Time Off (PTO) or Flexible Time Off (FTO)
• Tuition Reimbursement
• Employee Stock Purchase Plan

What This Job Offers

• Job Type: Full-time
• Industry: Ambulatory Health Care Services
• Education Level: Bachelor's degree