Job Description

Molecular Laboratory Technologist II

Nashville, TN

As a Molecular Laboratory Technologist II, you will perform high-complexity molecular diagnostic testing, adhering to CLIA, CAP, TN Medical Laboratory Board, and company protocols. Your focus will be on the accurate and timely analysis of patient samples using PCR and other molecular techniques to support our oncology-focused testing services.

Job Responsibilities:

• Perform clinical testing according to laboratory procedures for specimen handling, processing, test analysis, and reporting. Maintain accurate records of patient test results.
• Operate and maintain laboratory equipment, including performing routine maintenance (daily, weekly, monthly, etc.) and coordinating yearly calibration/preventive maintenance.
• Maintain a clean, safe, and orderly working environment.
• Conduct quality assurance activities such as proficiency testing, instrument/method comparisons, and reagent qualifications.
• Adhere to quality control procedures and actively participate in quality improvement initiatives.
• Troubleshoot and resolve assay or equipment issues, escalating complex problems to Laboratory Management.
• Contribute to maintaining sufficient inventory of reagents and consumables.
• Assist in writing and revising Standard Operating Procedures (SOPs), offering recommendations for improvements.
• Provide support in training new laboratory staff members.
• Comply with all safety guidelines and procedures.
• Support the company's goals, including performing CLIA validation studies as needed.
• Manage assigned projects with moderate supervision, potentially leading smaller projects.

Job Requirements:

• Current State of Tennessee Department of Health Medical Laboratory Technologist License (Generalist) or Special Analyst Molecular Diagnostics License OR ASCP Certification.
• Bachelor’s Degree (minimum) in a chemical, biological, clinical, or medical laboratory science.
• 2+ years of clinical laboratory experience performing high-complexity testing.
• Demonstrated understanding of Good Laboratory Practice (GLP) and Good Documentation Practice (GDP).
• Strong micro-pipetting skills.
• Preferred experience in molecular diagnostics (e.g., Real-Time PCR, Droplet Digital PCR, Next Generation Sequencing).
• Preferred experience working with a Laboratory Information Management System (LIMS) and Electronic Document Management System (EDMS).
• Excellent interpersonal skills with a proven ability to work effectively in a team.
• Ability to thrive in a fast-paced and evolving environment, demonstrating flexibility and adaptability to changing priorities.

Job Details:

• Work Schedule: Tuesday-Saturday; 6;00am -2:30pm OR 6am2:00pm-10:30pm (Subject to Change)
• Training: M-F; 9am-5:30pm
• Require to work holidays per Clinical Operations Schedule Policy.
• Flexible and open to occasionally working alternate shifts to support coverage requirements.

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