Molecular Technologist / Laboratory Consultant (Part-Time)

Key Responsibilities

Provide technical consultation for molecular diagnostic testing, including PCR, RT-PCR, NAAT, and other molecular platforms Review, approve, and oversee test validations, standard operating procedures (SOPs), quality control, and quality assurance processes Ensure compliance with CLIA, COLA, CAP, and all applicable federal, state, and local laboratory regulations Assist with laboratory inspections, audits, proficiency testing, and regulatory documentation Review and approve test reports, workflows, validation summaries, and technical documentation as required Provide guidance on assay development, verification, validation, and implementation of new tests Support troubleshooting of molecular instruments, automation systems, and testing processes Collaborate with the Laboratory Director, Medical Director, and leadership on regulatory, technical, and operational matters Be available for consultation as required to maintain compliance for high-complexity testing under CLIA regulations Maintain appropriate documentation to support role as Technical Consultant / General Laboratory Supervisor / Technical Supervisor , as applicable under CLIA/CAP requirements Participate in quality management activities, including corrective actions, competency review, and performance monitoring Onsite presence required a minimum of one (1) day per week , and additional onsite availability during validations, inspections, audits, or other key regulatory activities Platforms Used The consultant will provide technical oversight and support for the following laboratory platforms and automation systems: Thermo.

Fisher Quant. Studio 12K Flex Thermo. Fisher Quant. Studio 5 MSGI Liquid Handler Automation System MSGI Decapper Automation System King. Fisher Extraction System Integra Automated Pipetting System Minimum Qualifications Master’s degree in Molecular Biology, Medical Laboratory Science, Clinical Laboratory Science, Microbiology, or related scientific field Prior experience in a CLIA-certified high-complexity laboratory Strong knowledge of CLIA, COLA, CAP, and other applicable laboratory regulatory standards Experience with molecular testing methods including PCR, RT-PCR, NAAT, sequencing, or equivalent technologies Experience reviewing and approving validations, SOPs, quality systems, and technical procedures Ability to serve in a Technical Consultant, Technical Supervisor, or General Laboratory Supervisor capacity as defined under CLIA/CAP regulations Strong documentation, regulatory compliance, and inspection-readiness skills Ability to work in a part-time consultant role with onsite presence as required About Trilab Health Trilab Health is a physician-founded and physician-led clinical laboratory dedicated to delivering high-quality diagnostic services with unmatched precision, transparency, and care.

Headquartered in the Chicagoland area, our team brings years of clinical, operational, and laboratory expertise across toxicology, molecular diagnostics, general chemistry, and hematology. We partner with healthcare providers, treatment centers, and medical practices across the country to support better patient outcomes through reliable testing and exceptional service.

Since our inception in 2015, our focus has remained clear: provide accurate, timely diagnostics while building meaningful relationships with the providers and patients we serve. With industry-leading turnaround times, robust internal quality processes, and a commitment to integrity, Trilab Health continues to set the standard for excellence in clinical laboratory testing.

WHY CHOOSE US Our Mission At Trilab Health, our mission is to empower healthcare providers with precise diagnostics, clear insights, and compassionate support so they can make informed decisions that improve patient care. We strive to be more than a laboratory—we are a trusted partner in driving better health outcomes, advancing compliance, and elevating the patient experience.