LC-MS/MS Toxicology Laboratory Supervisor

LC-MS/MS Toxicology Laboratory 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 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 Responsibilities 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 MassHunter 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 Required Qualifications 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 MassHunter for data acquisition, analysis, and reporting Documented experience in LC‑MS/MS method development and validation in a clinical or regulated laboratory setting Proficiency with sample preparation techniques, including dilute‑and‑shoot, solid‑phase extraction (SPE), and liquid‑liquid extraction (LLE) Strong knowledge of quality assurance, quality control principles, and corrective action processes Demonstrated knowledge of CLIA high‑complexity testing regulations, OSHA safety requirements, and regulatory compliance 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, lead, or certifying scientist capacity Experience developing or delivering competency assessments for laboratory staff Experience with Beckman Coulter AU 480/680 or equivalent Beckman Coulter AU‑series chemistry analyzers (e.g., AU400, AU5800) Experience with additional LC‑MS/MS platforms (e.g., SCIEX, Shimadzu, Thermo Fisher) Experience supporting CAP accreditation, laboratory audits, and regulatory inspections Familiarity with Laboratory Information Systems (LIS) and electronic reporting workflows Ability to design and deliver technical training programs for laboratory staff Experience with high‑throughput batch processing workflows in a clinical toxicology environment ASCP MLS(ASCP), AMT MT, NRCC, or other relevant certification Master's degree in chemistry, toxicology, clinical laboratory science, or a related field Benefits for full‑time W2 Team Members Benefits begin 60 days after the first full month of full‑time employment. Health, Dental, and Vision Insurance Paid Time Off (21 days annually for full‑time team members) 7 Paid Holidays 401(k) with 50% Company Match up to 6% Health Savings Account (HSA) Short‑Term & Long‑Term Disability (RML covers 60% of STD premium) Voluntary Life and AD&D Insurance 100% Company‑Funded Employee Assistance Program (EAP) If you meet the above qualifications and are interested in joining our team, please submit your resume for consideration. We look forward to hearing from you! Equal Opportunity Employer Statement Rocky Mountain Laboratories is an Equal Opportunity Employer committed to diversity in its workforce. We comply with all applicable federal and state laws and prohibit discrimination based on race, ethnicity, religion, color, national origin, sex, age, sexual orientation, gender identity or expression, veteran status, disability, or genetic information. We also comply with the Americans with Disabilities Act (ADA) and provide reasonable accommodations to qualified individuals with disabilities. #J-18808-Ljbffr