Rocky Mountain Laboratories LLC
Location
Draper, Utah
Salary
$31 - $38 / HOUR
Perform full-cycle clinical toxicology testing, including immunoassay screening and LC-MS/MS confirmatory analysis for drugs of abuse and therapeutic drug monitoring. Responsible for specimen preparation, instrument operation, data review, and maintaining strict quality control and documentation standards.
Requires a Bachelor's or Associate degree in a laboratory science or related field and at least one year of high-complexity clinical toxicology experience in a CLIA-certified lab. Must have hands-on LC-MS/MS experience and be able to pass a post-offer drug screen.
Location: Draper, UT — reliable commute or relocation required before start date
Full-cycle clinical toxicology testing — immunoassay screening and LC-MS/MS confirmatory analysis for drugs of abuse (DOA), pain management, and therapeutic drug monitoring (TDM) panels Specimen preparation for urine and oral fluid samples per established SOPs (dilute-and-shoot, aliquoting, filtration, and related techniques) Batch setup, loading, and processing on triple quadrupole mass spectrometry and chemistry analyzer platforms Instrument operation, calibration, and routine/preventive maintenance — including Agilent 6460 triple quadrupole LC-MS/MS and Beckman Coulter AU 480/680 (experience on these platforms is a strong plus) Data review — evaluating calibration curves, QC data, and patient results for accuracy and acceptability prior to release Identification and resolution of anomalies, interferences, QC failures, and out-of-range results; initiating reruns and corrective actions Reagent, calibrator, control, and standard solution preparation per laboratory procedures Accurate and complete documentation: instrument logs, maintenance records, QC charts, and batch records Inventory monitoring and proactive communication of reorder needs Participation in QA activities, proficiency testing, and continuous improvement initiatives Support for method validation and verification activities as directed Collaboration with team members and supervisors on assay, workflow, and instrumentation troubleshooting Required Qualifications: Bachelor's degree in medical laboratory science, clinical laboratory science, chemistry, biology, or a closely related field — OR — an Associate degree in laboratory science or medical laboratory technology from an accredited institution (with 6 credits chemistry, 6 credits biology, and 12 additional credits in either) At least 1 year of hands-on experience performing high-complexity clinical toxicology testing in a CLIA-certified laboratory (drugs of abuse, pain management panels, or TDM) Hands-on LC-MS/MS experience in a clinical or regulated laboratory environment Documented clinical lab training or equivalent experience per CLIA §493.1489 Strong attention to detail, organizational skills, and analytical thinking Proficiency with Microsoft Excel Ability to pass a post-offer drug screen — required for all personnel working in a federally regulated drug testing laboratory per applicable CLIA and federal guidelines
Experience on Agilent 6460 triple quadrupole LC-MS/MS and/or Beckman Coulter AU 480/680 or equivalent chemistry analyzer platforms Proficiency with Agilent MassHunter or comparable mass spectrometry data analysis software Experience with sample preparation techniques for LC-MS/MS (dilute-and-shoot, solid-phase extraction, liquid-liquid extraction) ASCP MLS(ASCP) or AMT MT certification Strong working knowledge of CLIA regulations, CAP standards, and QC practices Experience with laboratory information systems (LIS) and electronic result reporting Familiarity with batch processing and high-throughput sample workflows in a clinical toxicology setting 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) Ideal start date: As soon as possible Application Deadline: Applications are reviewed on a rolling basis, and the position may be filled before any stated deadline. 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! At Rocky Mountain Laboratories, we prioritize the care and well-being of our team members. 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. Pre-Employment Notice & E-Verify Rocky Mountain Laboratories participates in E-Verify. Employment is contingent upon successful completion of a background check and other pre-employment screenings, as required. Employment with Rocky Mountain Laboratories is at-will. This means either the Team Member or the company may end the employment relationship at any time, with or without cause or notice, in accordance with applicable laws. Nothing in this posting or in future communications alters that relationship. While we appreciate interest from staffing agencies, Rocky Mountain Laboratories does not currently partner with external agencies. Resumes submitted unsolicited will not be considered, and no fees will be paid. Please only reference our LinkedIn and Indeed pages for current openings: www.linkedin.com/company/rocky-mountain-laboratories www.indeed.com/cmp/Rocky-Mountain-Laboratories www.rockylabs.com
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