Medical Laboratory Technologist CLS/MLT

MFM HealthMiddleton, MA
$34 - $48Onsite

About The Position

MFM Health is seeking qualified candidates to join our laboratory team. The Medical Laboratory Technologist performs moderate-complexity laboratory testing in accordance with Massachusetts 105 CMR 180.000, CLIA regulations, and applicable federal and state requirements. This role is responsible for all phases of testing, including pre-analytical, analytical, and post-analytical processes, ensuring the accuracy, reliability, and integrity of laboratory results. The Technologist operates under the direction of the Laboratory Manager/Technical Supervisor and Laboratory Director, and may only perform testing for which they have been trained and demonstrated competency.

Requirements

  • Bachelor’s degree in Medical Technology or Medical Laboratory Technologist (Associates Degree)
  • Minimum 3 years of full-time clinical laboratory experience in chemistry, hematology, and microbiology preferred
  • 1–3 years of clinical laboratory experience in chemistry, hematology, and microbiology preferred.
  • Experience with laboratory diagnostic instruments such as Sysmex, Abbott Architect, and Cepheid
  • Experience with Laboratory Information Systems (LIS), including Orchard or equivalent systems
  • Familiarity with electronic health record (EHR) integrations and laboratory workflows
  • Must meet CLIA personnel requirements for moderate-complexity testing
  • Must demonstrate training and competency prior to performing testing independently

Nice To Haves

  • MT or MLS certification through ASCP or equivalent preferred

Responsibilities

  • Perform accurate and appropriate moderate-complexity testing according to established laboratory procedures.
  • Evaluate specimens for acceptability, ensuring proper labeling and identification, investigating and documenting unacceptable specimens, and handling and storing specimens according to required conditions and protocols.
  • Organize workload efficiently to ensure timely completion of testing and verify that test results correspond to the correct patient and specimen prior to release.
  • Report results accurately and within established turnaround times, following protocols for critical value identification and notification, documentation of communication with providers, and correcting erroneous results.
  • Report state-required reportable diseases to the Massachusetts State Laboratory Institute and document appropriately in the LIS.
  • Participate in periodic review of laboratory procedures and assist in updates as needed to ensure accuracy and compliance.
  • Perform and document quality control procedures, calibration, and instrument checks, ensuring quality control is acceptable before reporting patient results.
  • Accurately evaluate quality control results, document all results, and follow established protocols for failures, escalating unresolved issues.
  • Hold patient testing and reporting when quality control is outside acceptable limits.
  • Adhere to all regulatory requirements: Massachusetts 105 CMR 180.000, CLIA, OSHA and HIPAA.
  • Perform routine and scheduled maintenance activities, including daily, weekly, and monthly tasks as required, and calibration and calibration verification.
  • Document all maintenance and calibration activities and ensure instruments are functioning properly prior to use.
  • Troubleshoot issues related to instruments and equipment, reagents and quality control failures, and patient specimens.
  • Follow established troubleshooting protocols, document all steps taken and corrective actions, and notify Laboratory Manager or Technical Supervisor when issues cannot be resolved.
  • Adhere to all Universal Precautions and laboratory safety protocols, use appropriate Personal Protective Equipment at all times, and follow policies for chemical handling, biohazard disposal, and exposure prevention.
  • Maintain a clean and safe work environment, including disinfection of work surfaces and proper waste disposal, and report safety hazards immediately.
  • Maintain familiarity with Safety Data Sheets and spill response procedures for biological and chemical exposures.
  • Accurately document patient testing, quality control results, maintenance and calibration, and corrective actions, ensuring all records are complete, organized, and audit-ready.
  • Maintain documentation in accordance with retention requirements.
  • Maintain appropriate inventory levels of reagents and supplies, ensuring proper storage conditions, monitoring of expiration dates, and removal of expired materials.
  • Perform regular inventory checks and notify appropriate personnel for reordering.
  • Maintain clean, organized work areas.
  • Perform testing only within scope of training and documented competency.
  • Participate in initial training and ongoing competency assessments.
  • Follow direction from the Laboratory Manager or Technical Supervisor.
  • Do not perform high-complexity testing unless specifically authorized.
  • Communicate effectively with providers and clinical staff, including nursing and medical assistants, to support safe and effective specimen collection and testing workflows.
  • Collaborate with laboratory team members to support workflow.
  • Escalate clinical, operational, or compliance concerns appropriately.
  • Document relevant issues, observations, and process concerns in appropriate logs or systems to ensure continuity of information across laboratory staff.

Benefits

  • Discretionary paid time off
  • 401(k) plan with employer match
  • Continuous opportunities for learning and career advancement
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