Laboratory Medical Director, Molecular Pathologist

Essential Duties and Responsibilities: Ensure all Clinical Laboratory duties are properly performed; Must be accessible to the Clinical Laboratory to provide onsite, telephone or electronic consultation as needed; Ensure that the testing systems developed and used for each test performed in the laboratory provide quality laboratory services for all aspects of test performance, which includes the pre-analytic, analytic and post-analytic phases of testing; Guarantee that the physical and environmental conditions of the Clinical Laboratory are appropriate for the testing performed and provide a safe environment in which employees are protected from physical, chemical and biological hazards; Ensure that test methodologies selected have the capability of providing the quality of results required for patient care; Confirm that verification procedures used are adequate to determine the accuracy, precision, and other pertinent performance characteristics of the method; Verify that laboratory personnel are performing the test methods as required for accurate and reliable results; Act as temporary Laboratory Director in the absence of the license holder Laboratory Director, and at such time shall fully discharge the onsite duties and responsibilities of the Laboratory Director; Delegate the responsibilities of the Technical Supervisor, General Supervisor, Clinical Consultant, and Testing Personnel to employees who are qualified to perform such duties; Ensure that the Clinical Laboratory participates in a suitable accuracy assessment (proficiency testing) program and that: The results are returned within the timeframes established by the proficiency testing program; All proficiency testing reports received are reviewed by the appropriate staff to evaluate the laboratory's performance and to identify any problems that require corrective action; An approved corrective action plan is implemented when any proficiency testing result is found to be unacceptable or unsatisfactory; Ensure that the quality control and quality assessment programs are established and maintained to assure the quality of Clinical Laboratory services provided to identify failures in quality as they occur; Ensure the establishment and maintenance of acceptable levels of analytical performance for each test system; Ensure that all necessary remedial actions are taken and documented whenever significant deviations from the Clinical Laboratory's established performance characteristics are identified, and that patient results are reported only when the system is functioning properly; Ensure that reports of test results include pertinent information required for interpretation; Ensure that consultation is available to the Clinical Laboratory's clients on matters relating to the quality of the test results reporting and their interpretation concerning specific patient conditions; Ensure that a General Supervisor provide on-site supervision of high complexity testing; Ensure that a sufficient number of laboratory personnel are employed with the appropriate education and either experience or training to provide appropriate consultation, properly supervise and accurately perform tests and report test results in accordance with the personnel responsibilities; Ensure that prior to testing patients' specimens, all personnel have the appropriate education and experience, received the appropriate training for the type and complexity of the services offered, and have demonstrated that they can perform all testing operations reliable to provide and report accurate results; Ensure that all policies and procedures are established for monitoring individuals who conduct pre-analytical, analytical, and post-analytical phases of testing to assure that they are competent and maintain their competency to process specimens, perform test procedures and report test results promptly and proficiently, and whenever necessary, identify needs for remedial training or continuing education to improve skills; Ensure that an approved procedure manual is available to all personnel responsible for any aspect of the testing process; Ensure that the responsibilities and duties of each consultant and each supervisor, as well as each person engaged in the performance of the pre-analytical, analytic, and post-analytic phases of testing are specified in writing and identifies which examinations and procedures each individual is authorized to perform, whether supervision is required for specimen processing, test performance or result reporting and whether supervisor or director review is required prior to reporting patient test results; Perform biennial review of Standard Operating Procedures; and Report all concerns of test quality and/or safety to the Laboratory Supervisor or Safety Officer.

Qualifications: Must be a Doctor of Medicine or Doctor of Osteopathy licensed to practice medicine or osteopathy in the State of California; OR Must be certified in Anatomic or Clinical Pathology, or both, by the American Board of Pathology or American Osteopathic Board of Pathology or possess qualifications that are equivalent to those required for such certification; OR Have at least one year of laboratory training during medical residency (for example, physicians certified either in hematology or hematology and medical oncology by the American Board of Internal Medicine); OR Have at least two years of experience directing or supervising high complexity testing; OR Hold an earned doctoral degree in a chemical, physical, biological or clinical laboratory science from an accredited institution and Be certified and continue to be certified by a board approved by HHS; OR Before February 24, 2003, must have served or be serving as a director of a laboratory performing high complexity testing and must have at least Two years of laboratory training or experience, or both; and Two years of laboratory experience directing or supervising high complexity testing OR Persons who on or before February 28, 1992, were qualified under State law to direct a laboratory in the State in which the laboratory is located. Must fulfill requirements stated in 42 CFR 493.1443 Must fulfill requirements stated in the College of American Pathologists Checklist Work Environment: Hours and days may vary depending on operational needs. Standing or sitting for long periods of time may be necessary. May be exposed to hazardous materials, blood specimens and instruments with moving parts, heating or freezing elements, and high-speed centrifugation.

Delegated Duties and Responsibilities: Refer to assigned Delegation of Responsibilities Form 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 efficiency, effectiveness, and quality of work. Hybrid Work Model: This section is applicable to onsite employees who are eligible for hybrid work location as specified by management and related policies. Guardant has defined days for in-person/onsite collaboration and work-from-home days for individual-focused time. All U.S. employees who live within 50 miles of a Guardant facility will be required to be onsite on Mondays, Tuesdays, and Thursdays. We have found aligning our scheduled in-office days allows our teams to do the best work and creates the focused thinking time our innovative work requires. At Guardant, our work model has created flexibility for better work-life balance while keeping teams connected to advance our science for our patients. The annualized base salary ranges for the primary location and any additional locations are listed below. This range does not include benefits or, if applicable, bonus, commission, or equity. Each candidate's compensation offer will be based on multiple factors including, but not limited to, geography, experience, education, job-related skills, job duties, and business need. Primary Location: Redwood City, CAPrimary Location Base Pay Range: $217,800 - $299,450 Other US Location(s) Base Pay Range: $217,800 - $299,450If the role is performed in Colorado, the pay range for this job is: $187,200 - $257,400 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. Guardant Health is committed to providing reasonable accommodations in our hiring processes for candidates with disabilities, long-term conditions, mental health conditions, or sincerely held religious beliefs. If you need support, please reach out to Peopleteam@guardanthealth.comA background screening including criminal history is required for this role. GH will consider qualified applicants with criminal arrest or conviction histories in a manner consistent with applicable law including but not limited to the LA County Fair Chance Policies and the Fair Chance Act (Gov. Code Section 12952).Guardant Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. All your information will be kept confidential according to EEO guidelines. To learn more about the information collected when you apply for a position at Guardant Health, Inc. and how it is used, please review our Privacy Notice for Job Applicants. Please visit our career page at: Summary

Location: Redwood City, CA; Palo Alto, CA

Type: Full time