Full Time

    Onsite

    About the job

    Cytotechnologist

    The Cytotechnologist is responsible for the screening and reporting of negative gynecological cytology cases, and identifying and referring abnormal cases to the pathologist. The cytotechnologist also maintains accurate quality control and quality assurance records. They will manage all daily operations of the cytology laboratory.

    Job Description

    • Responsible for the screening and reporting of negative gynecological cytology cases, and identifying and referring abnormal cases to the pathologist.
    • Maintain accurate quality control and quality assurance records.
    • Manage all daily operations of the cytology laboratory.
    • Promote the facility mission, vision, and values by effectively communicating them to others.
    • Coordinate and direct all administrative and laboratory procedures within the section.
    • Ensure department policies and procedures are in compliance with regulatory agencies, e.g., Joint Commission, College of American Pathologist (CAP), and CLIA.
    • Review quality of test results and quality control procedures, making judgments concerning results and taking appropriate action to maintain accuracy.
    • Responsible for the prompt, accurate, and efficient screening of gynecological specimens and reporting the diagnostic results.
    • Assist in evaluating new test and operating procedures.
    • Microscopically examine gynecological specimens to properly identify and classify all abnormal, precancerous, and cancerous changes.
    • Identify infectious agents including viral, fungal, and other parasitic organisms.
    • Identify endocervical components when present; recognize abnormal cell changes associated with radiation and chemotherapy changes.
    • Enter results into LIS and verify for report release.
    • Participate in training and orientation of new employees, as required and assigned.
    • Adhere to and participate in quality control procedures and document accordingly; participate in proficiency testing.
    • May participate in evaluating new instruments and products.
    • Ensure compliance with federal and state regulations.
    • Maintain policy and procedure manual.
    • Perform related duties as required.

    Requirements

    • Bachelor's degree from an accredited school of cytotechnology or certified by a certification agency approved by The Centers for Medicare & Medicaid Services (CMS) required or an Associates with one year internship in an accredited school of cytotechnology.
    • Licensure/Registered - CT (ASCP) American Society for Clinical Pathology (preferred).
    • Demonstrate knowledge of anatomy, pathology, and medical terminology and be able to screen and render a final diagnosis for normal gynecologic slides and refer abnormal slides to pathologist for final diagnosis.
    • At least three years of experience in a clinical lab setting (preferred).