LC-MS​/MS Toxicology Laboratory Supervisor

LC-MS/MS Toxicology Laboratory Supervisor

Rocky Mountain Laboratories – Draper, Utah

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.

Rocky Mountain Laboratories is seeking an experienced Clinical Toxicology Laboratory Supervisor with hands‑on Agilent LC‑MS/MS expertise and method development experience to lead our toxicology department in Draper, Utah, part of the Salt Lake City metro area.

This is a working supervisor role in a CLIA‑certified, high‑complexity toxicology laboratory. You’ll combine bench‑level technical work — including LC‑MS/MS method development and validation, instrument operation, and data review — with day‑to‑day departmental leadership: staff oversight, SOP development, QC program management, and regulatory compliance. You’ll serve as the primary technical and operational lead for the toxicology department and act as department representative in the absence of the Lab Manager.

Job Type: Full‑time, W2

Schedule: Monday–Friday | 8:00 a.m.–4:30 p.m. | Day shift

Salary: $130,000–$150,000 annually

Location: Draper, UT (Salt Lake City metro) — reliable commute or relocation required before start date

Start Date: As soon as the right candidate is found

• Supervise daily toxicology laboratory operations to ensure accurate, timely, and compliant high‑complexity testing
• Operate, calibrate, maintain, troubleshoot, and optimize Agilent 6460 triple quadrupole LC‑MS/MS instrumentation and related platforms
• Develop, validate, and implement new analytical methods for clinical toxicology panels including drugs of abuse (DOA), pain management, and therapeutic drug monitoring (TDM)
• Lead method verification, troubleshooting, and continuous optimization of existing assays
• Oversee sample preparation workflows for urine and oral fluid specimens
• Develop, implement, and maintain Standard Operating Procedures (SOPs) for validations, clinical testing, and regulatory compliance
• Review, interpret, and authorize release of patient test results using Agilent Mass Hunter and other laboratory software in accordance with laboratory policies and CLIA standards
• Manage quality control (QC) and quality assurance (QA) programs; investigate out‑of‑range results and deviations; implement and document corrective actions
• Monitor workflow, prioritize testing queues, and allocate staff resources to meet turnaround time expectations
• Train, mentor, and evaluate laboratory staff; develop and administer competency assessments and provide ongoing technical guidance
• Serve as CLIA General Supervisor for the toxicology department, ensuring full compliance with high‑complexity testing standards, OSHA safety requirements, and other applicable regulations
• Support internal inspections, CAP accreditation activities, audits, and regulatory readiness
• Collaborate cross‑functionally with Chemistry, Molecular, Client Services, and other departments to resolve operational and testing issues
• Drive continuous improvement initiatives related to workflow efficiency, quality outcomes, and cost reduction
• Ensure proper handling, storage, and disposal of hazardous and biological materials
• Serve as acting department leader in the absence of the Lab Manager
• Perform other duties as assigned

• Bachelor of Science or higher in chemistry, biology, clinical laboratory science, medical laboratory science, or a closely related field
• Minimum 2 years of documented hands‑on clinical toxicology experience in a CLIA‑certified high‑complexity laboratory, including experience with drugs of abuse (DOA), pain management panels, or therapeutic drug monitoring (TDM)
• Recent hands‑on experience operating, maintaining, and troubleshooting Agilent 6460 triple quadrupole LC‑MS/MS or equivalent Agilent 6400‑series instrumentation, including proficiency with Agilent Mass Hunter for data acquisition, analysis, and reporting
• Documented experience in LC‑MS/MS method development and validation in a clinical or…