PRN Medical Technologist ; Second Shift

Labcorp Drug Development, the world’s most comprehensive drug development company, dedicated to improving healthcare and improving lives. Our unique perspectives, built from decades of scientific expertise and precision delivery of the largest volume of drug development data in the world, along with our innovative technology solutions, help our clients identify new approaches and anticipate tomorrow’s challenges as they evolve.

Second Shift PRN/Casual

All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data.

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. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please .

• Perform assigned clinical laboratory testing accurately and in a timely manner.
• Resolve pending items. Retrieve and check specimens against pending list. Document specimen discrepancies. Notify laboratory management when specimen discrepancies are not resolved.
• Prepare workstation and instrumentation for assigned testing.
• Properly handle specimens and independently resolve technical specimen issues in preparation for analysis and specimen storage. Contact internal customers for clarification as needed.
• Operate instruments to perform testing in accordance with established written procedures.
• Perform routine testing and calculations as required.
• Resolve routine and non-routine assay problems.
• Ensure the validity of test results through the performance of established quality assurance and quality control procedures.
• Perform experiments, as scheduled, for evaluation of new Calibrator and/or QC lots.
• Summarize results of investigations and compile data for review by management.
• Document quality control results. Interpret quality control results according to Westgard rules or other established departmental procedures and accurately document biases, warnings and violations of control values.
• Document corrective action for unusual occurrences (e.g., QC violations, instrument related problems).
• Analyze proficiency testing survey samples as patient specimens.

• Receive, open and place in service all reagents/materials according to SOPs.
• Prepare and properly label reagent, quality control, calibrator material.
• Document implementation of new reagents/materials according to SOPs.
• Perform parallel testing, linearity’s, stability, other quality control practices needed to ensure validity of material prior to being placed into service.
• Perform inventory control of supplies and reagents as approved by management.

• When data is manually entered (e.g., QC, patient data) ensure peer review is performed and documented prior to release of results.
• Prepare proper documentation of test results and enter into the information system.
• Generate an appropriate audit trail for all activities.
• Document and communicate any result reporting problems or inconsistencies to laboratory management.
• Complete testing within the expected turnaround time to meet customers’ expectations.

• Ensure maintenance of instruments and equipment is performed according to manufacturer and SOP requirements, and documented according to SOP.
• Calibrate instruments, equipment and/or assays as required and document.
• Perform basic instrument and equipment troubleshooting.
• Perform pipette calibrations and document according to SOP.
• Notify laboratory management when an instrument or equipment does not meet specifications.

• Comply with regulatory guidelines and Covance Standard Operating Procedures (SOPs) at all times.

• Individual is responsible for maintaining his/her complete up-to-date training file and is accountable…