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Laboratory Supervisor; Clinical Toxicology, LC-MS​/MS

Job in Draper, Salt Lake County, Utah, 84020, USA
Listing for: Rocky Mountain Laboratories
Full Time position
Listed on 2026-01-22
Job specializations:
  • Healthcare
    Clinical Research, Medical Technologist & Lab Technician, Medical Science
Salary/Wage Range or Industry Benchmark: 95000 - 120000 USD Yearly USD 95000.00 120000.00 YEAR
Job Description & How to Apply Below
Position: Laboratory Supervisor (Clinical Toxicology, LC-MS/MS)

Laboratory Toxicology Supervisor – Rocky Mountain Laboratories, Draper, Utah

About Us
Rocky Mountain Laboratories is a clinical laboratory providing comprehensive laboratory services. We are dedicated to delivering accurate and timely diagnostic information and are committed to improving healthcare outcomes through cutting‑edge technology and a customer‑focused approach.

Position

The Laboratory Toxicology Supervisor is responsible for leading day‑to‑day operations within the toxicology department, with a strong focus on clinical accuracy, regulatory compliance, and operational efficiency
. This role combines hands‑on technical expertise with supervisory leadership in a high‑complexity clinical toxicology laboratory
.

The successful candidate will oversee LC-MS/MS instrumentation
, method validation, quality control processes, and staff training while ensuring compliance with CLIA, CAP, OSHA
, and other applicable regulatory standards. This position serves as the primary technical and operational lead for toxicology testing and acts as the department representative in the absence of the Lab Manager.

Schedule

Full‑time, onsite in Draper, Utah
Monday to Friday 0800 to 1630 with some flexibility

Responsibilities
  • Supervise daily operations of the toxicology laboratory to ensure accurate, timely, and compliant testing
  • Oversee LC‑MS/MS and mass spectrometry instrumentation
    , including calibration, maintenance, troubleshooting, and method optimization
  • Develop, implement, and maintain Standard Operating Procedures (SOPs) for validations, clinical testing, and regulatory compliance
  • Review, interpret, and release patient test results in accordance with laboratory policies and regulatory requirements
  • Manage quality control (QC) and quality assurance (QA) programs; investigate out‑of‑range results and implement corrective actions
  • Monitor workflow, prioritize testing, and allocate staff resources to meet turnaround time expectations
  • Conduct internal laboratory inspections, audits, and regulatory readiness activities
  • Ensure compliance with CLIA high‑complexity testing
    , CAP standards, OSHA safety requirements, and other applicable regulations
  • Train, mentor, and evaluate laboratory staff; provide ongoing technical guidance and performance feedback
  • Collaborate cross‑functionally with Chemistry, Molecular, Client Services, and other departments to resolve operational or testing issues
  • Ensure proper handling, storage, and disposal of hazardous and toxic materials
  • Drive continuous improvement initiatives related to workflow efficiency, cost control, and quality outcomes
  • Serve as acting leader for the toxicology department in the absence of the Lab Manager
  • Perform other duties as assigned
Required Qualifications
  • Minimum 2 years of documented clinical toxicology experience in a regulated laboratory environment
  • Hands‑on experience with LC‑MS/MS instrumentation
    , including sample preparation and data analysis
  • Strong knowledge of quality assurance and quality control principles
  • Demonstrated ability to follow and enforce regulatory standards (CLIA, CAP, OSHA)
  • Excellent organizational, analytical, and problem‑solving skills
  • Strong written and verbal communication skills
  • Ability to manage multiple priorities while maintaining accuracy and compliance
Preferred Qualifications
  • 3–5+ years of clinical toxicology laboratory experience, including at least 1 year in a supervisory or lead role
  • Clinical toxicology experience in pain management
    , drugs of abuse, or therapeutic drug monitoring
  • Hands‑on experience with triple quadrupole mass spectrometry
  • Proficiency with Agilent 6460
    , Mass Hunter software, and Beckman AU 480/680 analyzers
  • Experience validating new assays and troubleshooting complex LC‑MS/MS methods
  • Familiarity with Laboratory Information Systems (LIS) and electronic reporting workflows
  • Experience supporting laboratory audits and regulatory inspections
  • Ability to design and deliver technical training programs
  • Master’s degree in chemistry, toxicology, clinical laboratory science, or a related field
Education

Bachelor of Science or higher in chemistry, biology, clinical laboratory science, or related field.

Job Type & Salary

Full‑time
$95,000 – $120,000 annually,…

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