Cytologist

PathGroup; Greenville (SC); On-site; USD 60,000 - 75,000; Full time

Job summary

PathGroup in Greenville, SC is seeking a Cytotechnologist to examine cells on glass slides to detect diseased, pre-malignant and malignant changes, following department protocols. Daily duties include reviewing gynecologic and non-gynecologic slides, recording findings in the LIS, maintaining logs, performing instrument maintenance, and contributing to QA/QC programs.

You will work within safety and privacy guidelines and support the Corporate Compliance Program while ensuring accurate reporting

Qualifications

• Bachelor's degree in Cytotechnology and ASCP certification are required or strongly preferred.
• Experience with gynecologic and non-gynecologic cytology is desirable.
• Proficiency with laboratory safety procedures and QA/QC processes.

Responsibilities

• Examine gynecological and non-gynecological slides daily according to department protocols.
• Record findings in computer system and update logs.
• Identify and correct problems affecting test performance or reporting.
• Perform instrument maintenance and troubleshooting as needed.
• Support QA/QC programs and ensure compliance with safety policies.

Skills

Cytology

Microscopy

Laboratory safety

Education

Bachelor's degree in Cytotechnology

ASCP Certification

Tools

Microscope

LIS

Slide staining

Job description

Job Summary

The person in this position is a Cytotechnologist who is responsible for examining cells on glass slides to detect evidence of diseased conditions and pre-malignant and malignant cells.

Essential Functions

• Examines gynecological and/or non-gynecological slides daily according to department protocols.
• Records findings in computer system.
• Records required data on daily screening and departmental logs.
• Identify and correct problems that may adversely affect test performance or result reporting of patient samples.
• Communicates pertinent section information/issues to supervisor, manager or other appropriate individual.
• Performs instrument maintenance and method troubleshooting.
• Assists in documentation and maintaining effective department QA/QC programs and monitors.
• Must perform within the productivity expectations as set forth by current departmental guidelines.
• Exercise all laboratory safety precautions and adhere to lab procedures as stated in procedure manuals.
• Perform all job responsibilities in alignment with the industry's best security practices and regulatory guidelines to protect the confidentiality, integrity, and availability of protected health information and other sensitive company data.
• Must be familiar with and abide by the Corporate Compliance Program and all Corporate policies, including the Privacy and Security policies.