MEDTOX Laboratories, located in St. Paul, is a drug testing and esoteric clinical laboratory with a focus on technology, quality and service to our clients. Established in 1983, MEDTOX is now the nation's third largest SAMHSA-certified drug testing laboratory. We are seeking a QA/QC Cytotechnologist Team Lead interested in contributing to our rapidly growing organization.

The QA/QC Cytotechnologist Team Lead performs microscopic evaluation of cytologic specimens with few discrepancies; has the ability to evaluate 60-70 GYN specimens daily; performs quality assurance/quality control and handles specimen preparation duties when required. Oversee the cytology department generating all monthly reports and statistics.

Primary Responsibilities:

• Perform microscopic evaluation of cytologic specimens with few discrepancies following laboratory procedures and workload policies. Verify the identification of the specimen; know technical limitations and the possibility of procedural error; consider diagnostic possibilities in result outcomes and potential ramifications in failed testing; identify problems when applicable.
  
• Perform quality assurance as requested; assume duties of cytology supervisor in their absence.
  
• Assume specimen preparation and microscopic diagnostic duties as required
  
• Prepare a final report using established terminology.
  
• Review, sign and date worksheets on all performed testing.
  
• Finalize testing results into the computer and ensure accuracy of information on reports.
  
• Maintain absolute integrity in the accurate performance and reporting of results and observes professional discretion with patient information. Follow and assist with implementation all HIPPA regulations.
  
• Hierarchical review and resulting of pap smears originally interpreted as “unsatisfactory” and/or “normal” in compliance with MEDTOX quality control/quality assurance guidelines.
  
• Maintain accurate QC and QA records as required by the laboratory and various regulatory agencies. Never exceed workload volumes established by Medical Director and Lab Director/Cytology Supervisor.
  
• Generate or assist in generating monthly department statistics and analysis and amended reports as requested; generate QC/QA reports for CLIA inspections.
  
• Write and/or assist with the writing of department policies, SOP’s and validations.
  
• Perform and/or assist with instrument and test validations.
  
• Assist in orientation/training of cytotechnologists.
  
• Maintain departmental equipment according to manufacture specification so that all testing is performed in optimal conditions.
  
• Participate in a proficiency-testing program selected and provided by the laboratory.
  
• Comply with all safety, infection control, and HIPPA policies.
  
• Contribute to departmental diagnostic expertise by sharing interesting cases.
  
• Participate in CAP inter-laboratory comparison programs and continuing education courses as needed
  
• Screening of all Liquid based cytology, including ThinPrep specimens both manual and imaged (Cytyc will train on imager)
  
• Assist with fine needle aspirations
  
• Assist with preparation for all inspections

Minimum Qualifications:

• Bachelor’s degree in cytotechnology or equivalent education or experience
  
• CT (ASCP certified)
  
• A minimum of five years relevant experience
  
• Maintain proficiency as a Technologist within the areas of responsibility (Cytotechnologist must pass proficiency testing annually)
  
• Intermediate to advanced knowledge of computerized systems and equipment relevant to this position
  
• Prior experience as a Quality Assurance/Quality Control Cytotech is preferred, but not required

Other Knowledge, Skills and Abilities:

• Strong analytical and problem solving skills
  
• Excellent attention to detail and accuracy
  
• Must be able to work independently
  
• Must pass national testing annually

Physical Demands/Working Conditions/Work Environment:
While performing the duties of this job, the employee is frequently required to sit and talk or hear. They may need to use hands to grasp or operate objects, tools or controls. The employee is occasionally required to climb, balance, stoop, kneel, crouch, reach with hands and arms, and walk; lift, push or pull objects. Hand-eye coordination is necessary to operate computers and other office equipment. Specific vision abilities required by this job include close vision and the ability to adjust focus. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

TO APPLY:

Please click link below to submit online application and resume.

QA/QC Cytotechnologist Team Lead