Quality Assurance Specialist

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 Clinical Lab Quality Assurance Specialist to join our team in  Tulsa, OK   Work Schedule:   Monday-Friday 8am-5pm Job Responsibilities   Supports supervisors with the review of quality control data to identify trends, problems, and accuracy issues Examines outlier results and QA exception reports thoroughly and within required timeframes. Maintains complete, accurate, and up-to-date records (logs, reports, worksheets, paperwork) for immediate access or timely retrieval. Creates and updates QA procedures and documentation that are clear, accurate, and user-friendly. Assists in process improvement and quality improvement initiatives; supports QA plan reviews and report generation Performs clerical and technical tasks such as data entry, report generation, communications, database maintenance, and filing. Participates in Lean activities (e.g., 5S) and ensures adherence to preventive maintenance and calibration schedules for equipment. Conducts high-complexity technical and non-technical testing per SOPs and protocols. Supports change control projects and assists with validations. Completes quality events in the Document Control system. Ensures compliance with CAP, CLIA, ISO, and other applicable regulations; supports audits and inspections. Manages training and competency programs for staff. Tracks, monitors, and presents operational and quality metrics to management. Initiates or supports corrective actions from audit observations and investigations; monitors effectiveness. Schedules and performs audits. Maintains documentation for regulated studies in compliance with applicable regulations. Oversees the proficiency testing program and ensures PT responses are submitted timely, processes PT evaluation, and facilitates PT failure investigation.

Bachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science or Medical Technology 2 years or more of previous experience as a Medical Technologist or in a quality related position  Preferred Qualification:   Current or prior Labcorp experience  Additional Job Standards   General knowledge of laboratory regulations (CAP/CLIA/ISO) and licensing requirements   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   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   Benefits:  Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to