The Position:

Under the direction of the Director of Cytology, the Cytotechnologist will be responsible for the daily technical and stain quality assessment, processing of Thyroid FNA (Fine Needle Aspiration) samples and go to for general technical questions. The Cytotechnologist uses scientific methods to solve problems and works closely with laboratory personnel to ensure patient samples are handled according to Standard Operating Procedures. This is an onsite position, and the schedule will be Tuesday - Saturday, 9:30am - 6:00pm.

• Adhere to and documents all quality control / quality assurance activities.
• Identify problems that may adversely affect test performance or reporting of results.
• Assist in the proper storage and maintenance of cytology records and samples.
• Assists in ensuring the laboratory is compliant with corporate, state, and federal regulatory requirements related to personnel safety and quality of the laboratory.
• Assists with developing and implementing laboratory procedures and installation of new equipment and methods.
• Maintains technical knowledge in cytopathology and/or histopathology.
• Ensure proper coverage and scheduling to maintain laboratory TAT expectations and KPI goals.
• Perform inspections and validations of methodology and instrumentation.
• Participates in all non-technical activities to support team members and operations, including Specimen Receiving, Accessioning, Processing, slide archival, etc.
• Perform daily stain and technical assessments of cytology and histology slides.
• Recommend action plans for Process Improvements.
• Promotes the continuous improvement of workplace safety and environmental/infection control standards and practice.
• Performs other duties as assigned.

Who You Are

Required Work Experience:

• Minimum 1 year as a Cytotechnologist.
• Bachelor’s degree in clinical lab, physical, or biological science.
• Meet state licensure requirements, if applicable.
• Certification is required:
  • Certified as a Medical Technologist, Medical Laboratory Scientist by the American Society of Clinical Pathology or equivalent

Preferred Work Experience:

• Minimum of 2-3 years as a Cytotechnologist with experience working in a high- complexity laboratory.
• Meet CLIA requirements (CFR.493. 1483).
• Liquid- based cytology training/certification preferred.

Other Skills and Attributes

• Excellent problem-solving skills; demonstrated strength intact and diplomacy with internal and external collaborators.
• Excellent written and oral communication skills.
• Ability to work independently and exercise good judgment.
• Excellent teamwork and collaborations skills.
• Excellent interpersonal skills.

What We Can Offer You

Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are proud to have been named a “Bay Area Top Workplace” for ten years in a row by the Bay Area News Group, based solely on employee feedback.

The anticipated base salary range for candidates who will work in Austin, Texas is $30.00 to $33.65 per hour. 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.

About Veracyte

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 Twitter (@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.