Clinical Laboratory Scientist (WED-SAT MN shift- 9pm - 7:30am)

Company Description

Guardant Health is a leading precision oncology company focused on guarding wellness and giving every person more time free from cancer. Founded in 2012, Guardant® is transforming patient care and accelerating new cancer therapies by providing critical insights into what drives disease through its advanced blood and tissue tests, real-world data and AI analytics. Guardant tests help improve outcomes across all stages of care, including screening to find cancer early, monitoring for recurrence in early-stage cancer, and treatment selection for patients with advanced cancer. For more information, visit guardanthealth.com and follow the company on LinkedIn, X (Twitter) and Facebook. 

Position Summary:

The Clinical Laboratory Scientist II is responsible for performing high complexity laboratory testing (Next generation DNA sequencing) on patient specimens, performing quality control and quality assurance procedures, interpreting and reporting patient results, and complying with all applicable local, state and federal laboratory requirements. The work requires keeping meticulous and organized records, excellent attention to detail, the ability to multi-task, and be flexible with tasks and schedules.

Shift Details: Wednesday-Saturday; MN 9pm-7:30am PT

Essential Duties and Responsibilities:

· Perform laboratory tests, procedures and analyses per the laboratory’s standard operating procedures.

· Review, interpret and report patient results in LIMS.

· Independently identify and troubleshoot high complexity problems that adversely affect the test performance.

· Perform, review and document laboratory quality control procedures.

· Document all corrective actions taken when test systems deviate from the laboratory’s established performance specifications.

· Perform and document routine preventive maintenance.

· Assist with training of new laboratory personnel.

· Maintain sufficient inventory of laboratory supplies for daily operations and prepare reagents required for testing.

· Perform and document reagent qualification per the approved protocols.

· Perform annual review of Standard Operating Procedures.

· Report all concerns of test quality and/or safety to the Laboratory Supervisor or Safety Officer.

· Participate in introduction of assay improvements, new assay configurations and validation.

· Perform other miscellaneous laboratory duties as assigned and assist others as time allows.

Qualifications:

· California Clinical Laboratory Scientist license.

· Bachelor of Arts or Science in Biomedical Laboratory Science, Clinical Science or related field.

· 2+ years' experience in a clinical laboratory.

· Working knowledge of local, state, and federal laboratory regulations.

· Able to integrate and apply feedback in a professional manner.

· Able to prioritize and drive to results with a high emphasis on quality.

· Ability to work as part of a team.

Work Environment:

· Employee may be required to lift routine office supplies and use office equipment.

· Majority of the work is performed in a desk/office environment; however, there may be exposure to high noise levels, fumes, and biohazard material in the laboratory environment.

· Ability to sit for extended periods of time.

AI & Digital Fluency

• Demonstrate curiosity, sound judgment, and the ability to critically evaluate and responsibly leverage AI-enabled tools in accordance with company policies, ethical standards, and regulatory requirements to improve the eff