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Technical Laboratory Specialist
1 month ago
We are seeking a highly skilled Technical Laboratory Specialist to join our team at Quest Diagnostics Incorporated. This role is responsible for planning, coordinating, and evaluating technical and operational activities in the laboratory.
Key Responsibilities- Coordinate and document competency testing to ensure completeness and timeliness.
- Work with supervisors to develop lists for new testing and alter current documents as required.
- Create new and altered documents.
- Track proficiency testing and ensure timely arrival and preanalytical processing of all proficiency test kits.
- Monitor turnaround times from arrival to placement of the kit in the testing department.
- Develop and maintain a database for tracking proficiency testing process.
- Review corrected reports data on a monthly basis and work directly with supervisors to develop corrective actions.
- Assist supervisors in preparedness for in-house, corporate, and accrediting agency inspections.
- Observe performance of technical SOPs covering each general bench site once annually.
- Tabulate positivity data and report to corporate entities as required.
- Perform hardcopy and electronic reporting to state, county, and local agencies.
- Maintain State reporting test file.
- Work directly with the Medical Director, Data Management, and electronic reporting personnel to ensure that patient data is properly represented on all report formats for testing from all sources.
- Review reports for all tests one time annually.
- Perform system tests of data transmission across within-laboratory electronic interfaces to ensure accuracy.
- Work with ITG and technical staff to test new interfaces.
- Monitor the performance of instrument-to-instrument accuracy, ensuring timeliness.
- Input and review comparative data, maintaining electronic and hardcopy records.
- Review equipment maintenance records on a monthly basis.
- Review calibration and maintenance records of handheld pipettes and automated pipette systems on a monthly basis.
- Review that all non-certified thermometers are checked against a reference (NIST certified) thermometer or perform the reference check.
- Review SmarTech data, providing a daily report.
- At least three years of experience in a Clinical Laboratory setting.
- LCMS experience and experience with LCMS validations preferred.
- Preferred experience in Government agency reporting.
- PC application skills in Microsoft Office, including Excel and Access.
- Master's degree in Chemistry or Biochemistry strongly preferred.
- Bachelor's degree in Chemistry or Biochemistry required.
Quest Diagnostics Incorporated is an equal opportunity employer and values diversity in the workplace. We offer a competitive salary and benefits package, as well as opportunities for career advancement and professional growth.
