Cytotechnologist

sanford; Bismarck (ND); On-site; USD 43,000 - 68,000; Full time

Job summary

Sanford Health is seeking a Cytotechnologist to prepare slides and prioritize specimen processing, with duties including FNA collection and cytology QA/statistics. You will examine specimens under a microscope to identify malignant or related abnormalities and report results following established protocols.

The role emphasizes accuracy, safety, and adherence to quality assurance practices. Typical hours are day shifts, with Monday–Friday schedule and no weekends.

Qualifications

• Graduated from an ABHES-accredited cytotechnology program or other HHS‑approved equivalent.
• Certified as a Cytotechnologist by ASCP or approved agency.
• Alternative qualifying history: two years in an approved program or equivalent with relevant cytotechnology training/experience.

Responsibilities

• Prepare slides of human cell samples and prioritize specimen preparation.
• Process and examine specimens under a microscope to identify malignant or related abnormalities.
• Report laboratory results using cytotechnology terminology per protocols.
• Maintain safety and quality standards in specimen collection and processing.

Education

ABHES-accredited cytotechnology program

ASCP cytotechnologist certification

History of cytology training/experience requirements

US healthcare setting familiarity

Job description

Sanford Health, the largest rural health system in the United States, is dedicated to transforming the health care experience and providing access to world-class health care in America's heartland.

Work Shift

8 Hours - Day Shifts (United States of America)

Scheduled Weekly Hours

40

Compensation

Salary Range: $31.00 - $49.50

Eligible for new hire sign-on bonus!

Union Position

No

Department Details

Monday-Friday 8:00am-4:30pm with no weekends or call

Participate in other cytology duties consisting of, but not limited to specimen processing, FNA collection, and cytology QA/statistics.

Summary

Prepares slides of human cell samples and prioritizes specimen preparation (via specimen processing and/or FNA collections), following established standards and practices. Processes and examines various specimens under a microscope to determine possible malignant or related abnormal conditions.

Job Description

Ensures the accuracy of specimen analysis in compliance with established quality assurance policies and procedures. Reports laboratory results, using current cytotechnology terminology, according to institutional protocols and principles. Maintain effective laboratory operations by adhering to standards of specimen collection, preparation, or laboratory safety. Utilizes a microscope to examine specimens collected from the human body to identify abnormal cells and other conditions. Demonstrate skill in use of equipment relative to position. Recognizes and minimize safety risks and complies with all safety practices and protocols.

Qualifications

• (1) Graduated from an Accrediting Bureau of Health Education Schools (ABHES) accredited school of cytotechnology or other organization by health and Human Services (HHS); or
• (2) Certified in cytotechnology by a certification agency approved by HHS (e.g. American Society of Clinical Pathology); or
• (3) Before September 1, 1992, have successfully completed two years in an accredited institution (12 semester hours in science, eight of which are in biology) and have 12 months training in an approved school of cytotechnology; or have received six months formal training in an approved school and six months' full-time experience; or
• (4) Before September 1, 1992, have achieved a satisfactory grade in an HHS proficiency test for cytotechnologists; or
• (5) Before September 1, 1994, have two years' full-time experience or equivalent within the preceding five years examining slides under the supervision of a physician certified in pathology and before January 1, 1969, be a high school graduate from six months cytotechnology training in a laboratory directed by a physician and completed two years fulltime supervised experience in cytotechnology before January 1, 1969; or
• (6) On or before September 1, 1994, have two years' full-time experience or equivalent within preceding five years in the United States (US) and on or before September 1, 1995, have either graduated from a Commission on Accreditation of Allied Health Education (CAHEA) approved school to be certified as a cytotechnologist.
• Must hold certification as a Cytotechnologist from the American Society for Clinical Pathology (ASCP) Board of Registry. Cytotechnologists certified after January 2004 are required to produce all documentation related to fulfilling the requirements of ASCP's Certification Maintenance Program (CMP).

Sanford is an EEO/AA Employer M/F/Disability/Vet.

If you are an individual with a disability and would like to request an accommodation for help with your online application, please call 1-877-949-5678 or send an email to [e-mail].