Quest Diagnostics

Cytotechnologist

ID 2024-57187
Category
Operations
Position Type
Regular Full-Time
Shift
Day
Location Address
2560 N Shadeland Ave
Location City & State
US-IN-Indianapolis
Workplace Category
On-site

Overview

Cytotechnologist - M-F 7:00am - 3:30pm

$7500 Sign On Bonus 

Performs microscopic examination of gynecologic and non-gynecologic slides for abnormal cellular changes.  Responsible for referring appropriate cases for hierarchical review.   Performs all duties in accordance with state and federal regulations.  Maintains appropriate workload and quality assurance records. 

Responsibilities

  • Under general supervision, examine microscopically and interpret gynecologic and non-gynecologic slides for infectious, reactive/reparative, and abnormal cells.  Refer appropriate cases for hierarchical review. 
  • Identify problems that may adversely affect test performance or reporting of results. Refer to supervisor/manager and document corrective action taken.  
  • Fulfill the responsibilities as listed in CLIA  (CFR 493.1485):  
    • Document interpretation results of each specimen examined or reviewed. 
    • For each 24-hour period, document the total number of slides examined or reviewed in the laboratory as well as the total number of slides examined or reviewed in any other laboratory or for any other employer. 
    • Document the number of hours spent examining slides in each 24-hour period. 
  • Maintain and provide evidence of all required qualifications including ASCP, state licenses and liquid-based cytology certification, as applicable.   
  • Maintain familiarity with CLIA regulations, as applicable to cytology. 
  • Maintain specimen integrity and patient identification of all samples examined. 
  • Enter and/or report results into the laboratory information system, as applicable. 
  • Maintain confidentiality of patient test results in accordance with HIPAA regulations. 
  • Adhere to and document required quality control activities. 
  • Comply with all corporate, safety, quality control, and quality assurance standards. 
  • Comply with all local, federal, CLIA, and CAP regulations 
  • Participate successfully in required training and competency assessment. 
  • Participate successfully in a CMS-approved proficiency-testing program annually, as applicable. 
  • Acquire and document the required number of continuing education hours annually. 
  • Perform other duties as assigned, (e.g., specimen processing, data entry) to include performing and documenting quality control rescreening, if qualified under CFR 493.1469 (Cytology General Supervisor Qualifications). 

Qualifications

QUALIFICATIONS

Required Work Experience:  

  • Meet CLIA requirements (CFR.493.1483). 
  • Meet state licensure requirements, if applicable. 
  • Meet ASCP requirements for Cytotechnologist (if not certified prior to employment, must pass ASCP registry within one year of start date). 

Preferred Work Experience:  

Liquid-based cytology training/certification (ThinPrep and/or Surepath), preferred. 

Physical and Mental Requirements:  

  • The normal performance of duties may require lifting and carrying objects: Objects 1 to 10 pounds are lifted and carried frequently; objects 11 to 25 pounds are lifted and carried occasionally; objects 36 to 50 pounds are seldom lifted or carried and objects over 50 pounds are not to be lifted or carried without assistance.  
  • Ability to stand and work at the bench for long periods of time.  
  • Frequent walking and/or standing.  
  • May be required to use a wide variety of manual tools and laboratory instruments and apparatuses all of which demand significant manual dexterity 

Knowledge:  

N/A

Skills:  

N/A


EDUCATION


LICENSECERTIFICATIONS
Current state licensure, if applicable(Required)
Liquid-based cytology training/certification (ThinPrep and/or Surepath)
Meet ASCP requirements for Cytotechnologist (if not certified prior to employment, must pass ASCP registry within one year of start date). (Required)
Meet CLIA requirements (CFR.493.1483). (Required)

EEO

Quest Diagnostics is an equal employment opportunity employer. Our policy is to recruit, hire and promote qualified individuals without regard to race, color, religion, sex, age, national origin, disability, veteran status, sexual orientation, gender identity, or any other status protected by state or local law. Quest Diagnostics observes minimum age requirements established by federal, state and/or local laws, and will ask an applicant for verification when deemed necessary. 

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