Clinical Lab Scientist ll - 3rd Shift

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.

• We Seek A Better Way:
  We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care
• We Make It Happen:
  We act with urgency, commit to quality, and bring fun to our hard work
• We Are Stronger Together:
  We collaborate openly, seek to understand, and celebrate our wins
• We Care Deeply:
  We embrace our differences, do the right thing, and encourage each other

The Clinical Laboratory Scientist II (CLS II) is responsible for performing high complexity clinical laboratory testing on patient specimens, reviewing and reporting patient results, performing quality control and quality assurance activities and complying with all applicable local, state and federal laboratory, quality, and safety requirements. The high complexity nature of the work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently and effectively in a team environment.

The main duties and responsibilities of the Clinical Laboratory Scientist II include the following, but not limited to:

• Perform molecular genetic testing on clinical specimens
• Exhibits confidence and high performance of all laboratory standard operating procedures for specimen handling, processing, test analyses, and recording of test results, including mild complexity troubleshooting procedures
• Demonstrate ownership and completion of assigned or assumed tasks, including e‑mails, paperwork and documentation, and nonconformances, in a timely manner with little supervision
• Contribute to and participate with activities associated with quality assurance, regulatory compliance, and continuous improvement (e.g., monthly QA meetings, inspections, etc.)
• Participate in assay validation projects
• Perform, review and document laboratory quality control procedures in accordance with the Quality Assurance Program
• Prepare reagents required for laboratory testing
• Engage in training
• Perform proficiency testing for the clinical tests
• Assist in research and validation activities
• Independently identify and troubleshoot issues that could potentially adversely affect test performance
• Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications
• Follow the laboratory’s standard operating procedures for quality and environmental health and safety and report all concerns of test quality and/or safety to the Lab Supervisor or Safety Officer
• Ensure all work is performed in accordance with local, state, and federal regulations and participate in all regulatory inspections
• Work cooperatively in a team environment supporting fellow laboratory and management staff
• Perform any other site/lab specific duties as assigned

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.

• Active California Department of Public Health Clinical Laboratory Scientist (CLS) license or Clinical Genetic Molecular Biology Scientist (CGMBS) license (no exceptions)
• Experience in high complexity clinical laboratory testing, preferably in molecular diagnostics
• Performance of molecular testing (PCR, Microarray, Sanger/NGS sequencing) a plus
• Has at least 2 years of experience in molecular laboratory that demonstrate proficiency and…