Molecular Training Specialist, Liquid Profiling (2nd Shift)

At Caris, we understand that cancer is an ugly word—a word no one wants to hear, but one that connects us all. That’s why we’re not just transforming cancer care—we’re changing lives.

We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: “What would I do if this patient were my mom?” That question drives everything we do.

But our mission doesn’t stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare—driven by innovation, compassion, and purpose.

Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.

Position Summary
Molecular Training Specialist is responsible for developing and executing training procedures for the molecular department.

Job Responsibilities

• Maintain regulatory compliance to all applicable regulatory requirements (FDA, CLIA, NYS, ISO, CAP, etc.)

• Maintains exceptional quality standards for all molecular analysis.

• Initializes, tracks and documents the creation of competency samples.

• Initializes, tracks and documents the progress of employee training, including the review of cap checklists.

• Assists in high complexity projects and process improvements.

• Initializes, tracks and documents continuing education hours.

• Meets all deliverables and goals set by department. Adheres to the laboratory’s quality control policies, documents all quality control activities, instrument and procedural calibrations and maintenance performed

• Documents all corrective action taken when a test system deviates from the laboratory’s established performance specifications.

• Assists with the tracking, accumulation, and computation of performance metrics to include turnaround times, issue reviews and case tracking.

• Documents and reviews all accreditation agency pre-inspection paperwork and mandatory checklists.

• Performs periodic audits within the Molecular Department to ensure we maintain compliance.

• Participate in Quality Control / Quality Assurance process improvements.

• Capture, trend and analyze quality data monthly. Drive identified actions.

• Provide departmental and companywide training on regulatory requirements and quality control processes.

• Accepts other duties as assigned.

Required Qualifications

• Bachelor's or Master's degree in a chemical, biological, clinical or medical laboratory science, or medical technology from an accredited institution.

• 2+ years clinical lab experience with at least 1 year being high complexity molecular testing.

• Strong knowledge of quality control and monitoring methodologies.

• Proficient in Microsoft Office Suite, specifically Word, Excel, Outlook, general working knowledge of Internet for business use, and skilled in operating office equipment such as fax machines and copiers.

Preferred Qualifications

• Master's degree in a chemical, biological, clinical or medical laboratory science, or medical technology from an accredited institution.

• Experience in FDA regulated industries.

• Ability to work in a fast-paced, deadline driven environment.

• Knowledge of laboratory safety procedures for biohazards and chemicals, as well as quality control procedures and regulations.

Physical Demands

• Will work at a computer some of the time as well as need to keep inventory and ordering records requiring the use of copiers, fax machines, and PDF scanners.

• Visual acuity and analytical skill to distinguish fine detail. Ability to pass a visual color discrimination test.

• Manual dexte