*10k SIGN ON BONUS* Cytology Mgr req78922 in Chantilly, VA at Quest Diagnostics

Date Posted: 11/13/2021

Job Snapshot

Job Description

Cytology Mgr - Chantilly, VA - Monday-Friday 7:30am-4:00pm (Rotational Weekends)

*10k SIGN ON BONUS* 

JOB SUMMARY:

Manager will support Cytology and Histology departments. Responsible for all QA/QC activities of the business unit.  The scope of these responsibilities include but are not limited to: compliance with CLIA ’88 regulations, CAP requirements, Quest policies and procedures, state laws applicable to Cytology, performing annual on-site visits, providing technical assistance/counseling, handling client visits and phone calls as necessary and overall responsibility for the business unit operations.

JOB RESPONSIBILITIES:

  1. Assure that ALL Federal, State and internal standards and regulations are followed.
  2. Prepare reports, as necessary, to document compliance with regulations.
  3. Monitor remedial actions necessary for compliance and regulatory agencies.
  4. Sign off on BU’s polices and workflow changes to ensure optimal performance and alignment with regulatory requirements.
  5. Review Quality Assurance/Control records to ensure compliance with regulations.
  6. Be responsible for maintaining BU’s performance and budget within set guidelines.
  7. Provide technical assistances and counseling in all areas regarding Cytology for all laboratories providing Cytology services for Quest Diagnostics.
  8. Provide assistance to clients through visits or phone consultations to maintain construction relationships and address issues requiring correction.

This is not an exhaustive or inclusive list of all the duties that may be required to this individual.

JOB REQUIREMENTS

Education Preferred:     

  • Bachelor’s degree and/or graduate of approved Cytotechnology program or equivalent.
  • Successful completion of the ASCP board of registry examination.
  • Recognized as a CT(ASCP) or meet the grandfather requirements as of Jan. 1990.

Work Experience:           

  • Minimum 5 years in a supervisory within a large lab (>100,000 tests per year).
  • Must include responsibility for meeting regulatory requirements, budget and capital expense objectives.