Cytologist Full Time Jobs (NOW HIRING)

The Position:

The Cytologist supports specimen processing of thyroid FNA specimens in the Cytology laboratory. Responsibilities include staining, preparing smears, and creating cell blocks. Ensures proper specimen handling and identification to maintain integrity. Maintains procedures, records, and quality assurance programs in accordance with CLIA, CAP, and NYS standards. Teaches and assists cytopreparatory staff and researches and develops new processes. This is a full time position, Tuesday - Saturday, 9:30am - 6:00pm. We are also open to a part time position, Tuesday - Saturday, 10:30am - 4:30pm.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

The main duties and responsibilities include the following, but not limited to:

• Performs the duties as the Cytology Technician in addition to the following:
• Serves as a role model and promotes the mission and vision of the organization.
• Reviews slides for technical and stain assessment and troubleshoots errors andinitiates corrective actions and documentation.
• Assists with developing and implementing laboratory procedures and installation of new equipment and methods.
• Maintains technical knowledge in cytopathology and/or histopathology.
• Performs and/or oversees various administrative functions as delegated by the Associate Director.
• Organizes workflow and prioritizes the workload as needed.
• Monitors laboratory procedures to ensure compliance with all applicable regulatory agencies.
• Ensure proper coverage and scheduling to maintain laboratory TAT expectations and KPI goals.
• Perform inspections and validations of methodology and instrumentation.
• Performs Competency Assessments of non-testing personnel.
• Participates in all non-testing activities to support team members and operations, including Specimen Receiving and Accessioning.
• Perform daily stain and technical assessments of cytology and histology slides.
• Familiar with liquid-based preparation technology.
• Recommends action plans for Process Improvements.
• Promotes the continuous improvement of workplace safety and environmental/infection control standards and practice.
• Assists with the maintenance of equipment, quality control, inventory management in accordance with Standard Operating Procedures.
• Performs other duties as assigned.
• Provides oversight of the laboratory inventory management to ensure appropriate inventory levels are maintained to meet workload.
• Strives to maintain a positive work environment.
• Demonstrates interpersonal skills required to successfully perform as a team member in a constantly changing environment.
• Respects and maintains the confidentiality of information relative to clients and patients.
• Leads projects, research, and validation activities as assigned.
• Understands and follows all safety guidelines.
• Familiar with CAP and CLIA regulations.
• Handling and disposing of hazardous and non-hazardous materials.
• Performs all other assigned duties as directed by management.
• Must be able to flex schedule to accommodate workload, including weekend coverage.
• Work cross-functionally throughout all areas of the laboratory to ensure continuous workflow.
• Key knowledge expert in all areas of the laboratory.
• Perform all duties according to guidelines outlined within the quality systems.
• Compliant with company policies, procedures, safety requirements and regulations.

Who You Are:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills and/or abilities required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

EDUCATION and/or EXPERIENCE

• Required: BA/BS degree; BS in chemical, physical, or biological science, or Cytotechnology preferred.
• Minimum 2 years of experience in a cytology laboratory.
• Required: Cytologist, CT(ASCP) certification. Certified for Board of Certification (BOC) by the American Society of Clinical Pathologists (ASCP)
• Knowledge of CLIA, New York, CAP and OSHA regulatory requirements

OTHER SKILLS AND ATTRIBUTES

• Exposure to general laboratory environment conditions
• Ability to follow detailed instructions and maintain accurate records
• Ability to follow detailed instructions and maintain accurate records
• Strong attention to detail and organization skills
• Basic computer skills, including data entry and use of LIMS
• Excellent problem-solving skills
• Excellent written and oral communication skills
• Ability to work independently and exercise good judgement
• Excellent teamwork and collaboration skills
• Excellent interpersonal skills
• Enthusiasm and an entrepreneurial spirit
• Demonstrated self-starter
• Excellent verbal and written communication skills
• The ability to navigate efficiently through, or have familiarity with, various laboratory information systems (LIS) and have proficiency in Microsoft Office products (Excel, Word, Access and PowerPoint)

PHYSICAL REQUIREMENTS

• Repetitive movement of hands, arms, and legs
• Ability to stand or sit for extended periods of time
• Manual dexterity and visual acuity for handling and processing specimens
• Ability to wear personal protective equipment, including glove, lab coats, and safety glasses
• Repetitive movement of fingers (typing and/or writing)
• Sitting, with occasional walking, standing, stooping, and moving about
• Occasionally required to lift to 25 pounds

The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.

Veracyte (Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide. Veracyte is based in South San Francisco, California. For more information, please visit www.veracyte.com and follow the company on X (@veracyte).

Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States.