Clinical Laboratory Scientist II

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 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 Position:

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 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 reporting 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

Who You Are:

REQUIREMENTS: QUALIFICATIONS

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

• 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 independence in a clinical laboratory setting

• Must have strong analytical and problem-solving skills

• Must be detail-oriented and comfortable with technology

• Must have excellent verbal and written communication skills

• Strong computer skills across diverse platforms

• Excellent interpersonal communication and team player attitude

• Ability to adapt to change and a rapid work pace

• Maintains continuing education units required by California Department of Health Services and New York State Department of Health

PHYSICAL REQUIREMENTS

• Repetitive movement of hands, arms and leg, fingers (typing and/or writing)

• Gripping/grasping

• Reaching above/below shoulder level

• Sitting, with occasional walking, standing, stooping and moving about

• Exposure to general office environment conditions

• Occasionally required to lift up to 25 pounds

Location: San Diego, CA (Onsite)

Schedule: Tuesday - Saturday 5:00am - 1:30pm PT

The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to years of experience, skillset, geographic location, 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.

Pay range
$47—$55 USD

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 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 Veracyte

Veracyte (Nasdaq: VCYT) is a global diagnostics company whose vision is to transform cancer care for patients all over the world. We empower clinicians with the high-value insights they need to guide and assure patients at pivotal moments in the race to diagnose and treat cancer. Our Veracyte Diagnostics Platform delivers high-performing cancer tests that are fueled by broad genomic and clinical data, deep bioinformatic and AI capabilities, and a powerful evidence-generation engine, which ultimately drives durable reimbursement and guideline inclusion for our tests, along with new insights to support continued innovation and pipeline development. For more information, please visit www.veracyte.com or follow us on LinkedIn or X (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.

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