Cytotechnologist

Company Description

Accu Reference Medical Lab is a state-of-the-art medical testing laboratory providing a comprehensive range of diagnostic, screening, and evaluative tests for diverse health conditions. The laboratory is certified under the federal Clinical Laboratory Improvement Amendments (CLIA) and operates in full compliance with all applicable regulations. Accu Reference Medical Lab uses the latest diagnostic technology and continuously updates its service offerings as new tests become available. Highly trained laboratory professionals with extensive experience ensure accurate and precise test results, supported by ongoing improvements in testing quality, data handling, and reporting. Accu Reference Medical Lab is an equal opportunity employer committed to fair and inclusive hiring practices.

Please make an application promptly if you are a good match for this role due to high levels of interest.

Role Description

The Cytotechnologist is a full-time, on-site role based in Linden, NJ. This role is responsible for preparing, screening, and interpreting cytology specimens to detect cellular abnormalities, including precancerous and cancerous changes, under the supervision of a pathologist. Daily tasks include reviewing slides using microscopy, correlating cytologic findings with clinical information, and documenting results in accordance with laboratory protocols and regulatory requirements. The Cytotechnologist collaborates with pathology and laboratory teams to ensure accurate reporting, participates in quality control and proficiency testing, and adheres to safety procedures and CLIA standards. The role also involves maintaining equipment, troubleshooting technical issues, and contributing to continuous improvement initiatives within the cytology laboratory.

Qualifications

• Strong laboratory skills in specimen preparation, slide staining, microscopy, and handling of cytology samples.
• Knowledge of pathology and cytopathology principles, including interpretation of gynecologic and non-gynecologic specimens.
• Experience with quality control, quality assurance, and compliance with CLIA and other regulatory standards.
• Certification or eligibility for certification as a Cytotechnologist (e.g., ASCP) and familiarity with laboratory medicine practices.
• Associate or Bachelor's degree in Cytotechnology or a related laboratory science field from an accredited program.
• Strong attention to detail, analytical skills, and ability to recognize subtle cellular changes and artifacts.
• Effective written and verbal communication skills and ability to work collaboratively in a multidisciplinary laboratory environment. xhyhwjd
• Commitment to ethical standards, patient confidentiality, and continuous professional development through ongoing education.