Cytotechnologist - RTD
Shift: 1st
Schedule: Mon - Fri, Hours TBD
JOB SUMMARY
Participates in the development of new methods, evaluates quality and provides guidance on correct use of cytology specimens and the interpretation of slides made from cytology specimens; compares to Pap testing, methodologies and results; and reviews slide staining. Helps guide product development to obtain the highest possible performance, works with *** Pathologists, and supports Quality Control (QC) method development for cytology specimens.
Responsibilities
Performs analytical techniques on specimens that originate from a variety of sources including cervical swabs, sputum, urine, other body fluids, and fine needle aspirates.
Qualifies incoming samples for testing.
Performs evaluation of immunocytochemistry (ICC) biomarkers for proof of concept, feasibility, verification and validation studies/activities associated with new product development.
Performs and evaluates cytology techniques like Pap staining and provides results to scientists on the project.
Maintains records as needed.
Provides suggestions to improve work processes.
Provides root-cause analysis and implements corrective action for reagent or instrument related issues that may arise in sample processing.
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each responsibility satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the responsibilities.
Formal Training/Education
Bachelor's Degree in Biological Sciences or related field. REQUIRED AND
Graduation from a CAAHEP (The Commission on Accreditation of Allied Health Education Programs) accredited cytotechnology training program. REQUIRED
Experience
7 years Cytology, including cytology techniques and methods. REQUIRED AND
Experience in a laboratory setting. REQUIRED AND
Gynecological experience. PREFERRED
Are equivalencies acceptable? No
Knowledge, Skills and Abilities
Knowledge of clinical testing methods.
Ability to work constructively and collaboratively with internal as well as external colleagues.
Knowledge of the principles of light microscopy, the operation and maintenance of standard laboratory equipment, and computer skills.
Organizing, problem-solving, and analysis skills including the ability to follow written procedures and to document work accurately and thoroughly.
Excellent written and verbal communication skills.
Ability to work with minimal supervision and work in a cross functional team environment.
Ability to troubleshoot and make informed accurate assessments.
Licenses and Certifications
Cytotechnologist (CT) American Society for Clinical Pathology (ASCP) certified. REQUIRED
Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
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