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Medical Laboratory Scientist I/Technologist I, Certified

ARUP Laboratories•Salt Lake City, UT

About The Position

ARUP Laboratories is hiring a Medical Laboratory Scientist I/Technologist I, Certified, for Clinical Toxicology 1 in Mass Spec Operations (MSO), Extraction. The position provides technical and non-technical laboratory services and performs routine and complex tests in an assigned clinical laboratory department to provide physicians with rapid, accurate results. The employee works under the direction of a specialist, lead, and/or supervisor. This role is not qualified to delegate supervisory duties for New York testing areas. The schedule is 7:00 AM–5:30 PM on a 7-on/7-off A-week rotation. Training is Monday through Friday, 7:00 AM–3:30 PM (variable), for approximately six weeks. The posting offers a $3,000 sign-on bonus and applicable relocation reimbursement; some conditions may apply. Applicants must meet the education and credential evaluation requirements. Candidates within one semester or quarter of completing a qualifying bachelor's degree may be considered if they have successfully completed the clinical rotation relevant to the duties. Such candidates may be hired as a Technician, Medical Laboratory Scientist in Training, at a minimum pay rate of $25.92 per hour, and would have six months to obtain certification; other restrictions may apply.

Requirements

  • Bachelor's degree in Clinical Laboratory Science, Medical Laboratory Science, or Medical Technology, with education and credentials subject to evaluation.
  • Candidates near completion of a qualifying bachelor's degree must have successfully completed the clinical rotation in the area of job duties.
  • Certification is required for the certified role.
  • Ability to perform the analytic processes for which the employee is qualified, trained, and competent.
  • Ability to comply with laboratory SOPs, ARUP policies and procedures, and applicable CDC and OSHA requirements.
  • Ability to use personal protective equipment in a biohazard laboratory environment.
  • Ability to perform the physical and visual tasks described, including stooping, reaching, occasional movement between work sites, fine motor work, close/far/peripheral vision, and color discrimination.
  • Continual assessment of current literature and best practices.

Responsibilities

  • Perform waived, moderate, and/or highly complex analytic processes independently when qualified, trained, and competent under laboratory SOPs.
  • Operate, calibrate, and troubleshoot laboratory instruments; ensure equipment functions properly and report or request service as appropriate.
  • Perform quality control procedures, maintain QC records and documentation, and resolve and document QC failures with corrective action.
  • Follow specimen collection, handling, transport, and recording procedures.
  • Process and verify data and enter results and explanatory or interpretive information into the laboratory information system in a timely manner.
  • Monitor QC and assist with data collection for quality assurance indicators as assigned.
  • Perform internal and external proficiency testing.
  • Meet output measures and assist with work in any section where current competency has been verified.
  • Recognize and report critical patient results according to established processes.
  • Recognize unexpected results, errors, and problems with patient tests and escalate them as required.
  • Evaluate potential causes of unexpected test results and understand the theory of laboratory procedures.
  • Correlate clinical and laboratory data with pathologic states to determine result validity.
  • Evaluate exceptions to established criteria and special circumstances involving specimen collection and integrity for their impact on testing.
  • Recognize appropriate and inappropriate selection of basic and complex laboratory tests.
  • Prioritize testing and coordinate general workflow in the assigned area.
  • Integrate and relate laboratory data to investigate discrepancies and contribute to their resolution.
  • Train new and current employees on procedures and policies.
  • Provide technical information or instruction to clients, employees, medical students, residents, peers, physicians, and the public as appropriate.
  • Maintain adequate inventory of reagents and supplies.
  • Direct workflow activities and review daily data reports as assigned.
  • Assess peers performing testing as a qualified observer after two years of experience, excluding New York testing.
  • Perform other duties as assigned.

Benefits

  • $3,000 sign-on bonus, subject to conditions.
  • Applicable relocation reimbursement, subject to conditions.

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