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Clinical Laboratory Scientist II

2 months ago


Vista California, United States Exagen Inc. Full time
Job Summary

Exagen Inc. is seeking a highly skilled Clinical Laboratory Scientist II to join our team in the Toxicology department. As a key member of our laboratory team, you will be responsible for operating a liquid chromatography/mass spectrometry platform for the quantitative analysis and reporting of MTXPG3, MTXPG5, HCQ, and HCQ/CQ.

Key Responsibilities
  • Prepare and quality control all chemical, reagents, calibration, standard, and Master solutions.
  • Ensure reagents/test kits have received dates, expiration dates, and opened dates.
  • Prepare samples for extraction.
  • Enter and finalize all results in LIMS in a timely manner.
  • Check all QC and individual results before reporting.
  • Maintain all records for QC and results.
  • Troubleshoot, maintain, and operate LCM instruments.
  • Maintenance and Quality Control of instruments.
  • Adhere to the laboratory's quality control policies, document all quality control activities, instrument, and procedural calibrations, and all maintenance performed.
  • Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance.
  • Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications.
  • Review/train on new procedures. Identify problems that may adversely affect test performance or reporting of test results, correct the problems encountered, or immediately notify the senior technologist or supervisor.
  • Participate in all applicable safety training sessions. Know the location and contents of the safety manual. Know the location/use of all applicable safety equipment.
  • Review QC for each assay in Toxicology.
  • Complete L-J charts and review for each test monthly.
  • Train other laboratory staff or personnel to perform assays or operate instrumentation as requested.
  • Resolve routine and non-routine assay problems and ensure the validity of test results through the performance of established quality assurance and quality control procedures.
  • If applicable, answer questions from customers or other lab personnel.
Requirements
  • Ability to work Tuesday to Saturday (8:00 AM - 4:30 PM or 9:00 AM - 5:30 PM) and requires the ability to work a flexible schedule and overtime hours or weekend as needed.
  • Must be able to use general office equipment including computer, telephone, copier, etc.
  • Good organizational and interpersonal skills.
  • Bachelor's degree in a chemical, physical, biological, or clinical laboratory science, or medical technology from an accredited institution.
  • Or have earned an associate degree in laboratory science, or medical laboratory technology from an accredited institution.
  • At least 2 years' experience in the general lab or relevant lab experience.
  • CLS License.
  • Understanding of the field of toxicology.
  • 1-3 years of LC-MS required.