Specimen Processor

Veracyte•San Diego, CA

1d•$22 - $24•Onsite

About The Position

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven environment. This is what we call the Veracyte way – it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions. Our Values: We Seek A Better Way: We pursue bold ideas, embrace complexity, and keep pushing forward. We Make It Happen: We act with urgency, deliver with excellence, and always find a way. We Are Stronger Together: We engage with empathy, align around what's best for Veracyte, and celebrate as one team. We Care Deeply: We show up with integrity, kindness, and respect for one another. The Position: Primarily responsibility for receiving and accessioning specimens, handling specimen documentation, and data entry of requisitions. They are also responsible for keeping the lab in a clean and orderly condition. Specimen Processor I are knowledgeable in sample integrity issues and are a resource to others in the lab. They maintain flexibility regarding work schedules including daily assignments, holiday schedules, and days of the week as determined by business need.

Requirements

0-2 years of accessioning experience and/or in a lab setting
High school diploma or equivalent required
Good 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).
Good judgment and problem-solving skills
Excellent teamwork and collaborations skills
Ability to work independently

Nice To Haves

Bachelor’s degree preferred.

Responsibilities

Accessioning clinical specimens upon receipt and entering data into LIS system.
Specimen verification, labeling, tracking, and all related clerical functions.
Capable of identifying specimen processing problems that may adversely affect the reporting of test results and immediately notifying the supervisor.
Documenting all corrective actions taken when test systems deviate from the laboratory's established performance specifications.
Following the laboratory's established policies and procedures.
Understanding of compliance regulations related to test ordering.
Compliant with company policies, procedures, safety requirements and regulations.
Contributing to the safety of the laboratory operations by complying with established safety procedures and making recommendations for improvement.
Engaging in training and competency assessments.
Attending and participating in department meetings.
Participating in activities associated with regulatory compliance and inspections.
Assisting in continuous improvement activities/projects.
Assisting in research and validation activities.
Helping perform weekly, monthly, and other periodic room and equipment maintenance procedures in accordance with standard operating procedures.
Helping track and stock laboratory supplies.
General clean-up tasks, e.g. break down and trash shipping boxes/packaging, disinfect lab benches and surfaces, and put away supplies.
Working cooperatively in a team environment and supporting senior laboratory and management staff.
Working cross-functionally with Customer Care regarding specimen issues and Accessioning requests.
Complete other related administrative duties, including printing, copying, filing, faxing, and quality control of spreadsheets.