Veracyte
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 innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer careWe Make It Happen: We act with urgency, commit to quality, and bring fun to our hard workWe Are Stronger Together: We collaborate openly, seek to understand, and celebrate our winsWe Care Deeply: We embrace our differences, do the right thing, and encourage each otherThe Position:Location: This is an onsite position based in our San Diego location. The schedule is Sunday - Thursday 12:30 pm - 9:00 pm. 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.ESSENTIAL DUTIES AND RESPONSIBILITIES: The main duties and responsibilities of the Clinical Laboratory Scientist II include the following, but not limited to:Perform molecular genetic testing on clinical specimensExhibits 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 proceduresDemonstrate ownership and completion of assigned or assumed tasks, including e-mails, paperwork and documentation, and nonconformances, in a timely manner with little supervisionContribute 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 projectsPerform, review and document laboratory quality control procedures in accordance with the Quality Assurance ProgramPrepare reagents required for laboratory testingEngage in trainingPerform proficiency testing for the clinical testsAssist in research and validation activitiesIndependently identify and troubleshoot issues that could potentially adversely affect test performanceDocument all corrective actions taken when test systems deviate from the laboratory's established performance specificationsFollow the laboratory's standard operating procedures for quality and environmental health and safety and reporting all concerns of test quality and/or safety to the Lab Supervisor or Safety OfficerEnsure all work is performed in accordance with local, state, and federal regulations and participate in all regulatory inspectionsWork cooperatively in a team environment supporting fellow laboratory and management staffPerform any other site/lab specific duties as assignedREQUIREMENTS: QUALIFICATIONSTo 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.Who You Are:EDUCATION and/or EXPERIENCEActive 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 diagnosticsPerformance of molecular testing (PCR, Microarray, Sanger/NGS sequencing) a plusHas at least 2 years of experience in molecular laboratory that demonstrate proficiency and independence in a clinical laboratory settingMust have strong analytical and problem-solving skillsMust be detail-oriented and comfortable with technologyMust have excellent verbal and written communication skills Strong computer skills across diverse platformsExcellent interpersonal communication and team player attitudeAbility to adapt to change and a rapid work paceMaintains continuing education units required by California Department of Health Services and New York State Department of HealthPHYSICAL REQUIREMENTSRepetitive movement of hands, arms and leg, fingers (typing and/or writing)Gripping/graspingReaching above/below shoulder levelSitting, with occasional walking, standing, stooping and moving aboutExposure to general office environment conditionsOccasionally required to lift up to 25 pounds#LI-OnsiteThe 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.Pay range$51-$58 USDWhat We Can Offer YouVeracyte 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 thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose.About VeracyteVeracyte (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 (Formerly Twitter).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. View our CCPA Disclosure Notice.If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com