
Clinical Laboratory Scientist – Reporting, Tuesday-Saturday
Posted Sep 14

Posted Sep 14
This is a fully remote position, open to applicants in United States.
• Conduct advanced laboratory testing on patient specimens.
• Implement quality control and quality assurance protocols.
• Adhere to local, state, and federal laboratory regulations.
• Execute laboratory tests, procedures, and analyses following standard operating procedures.
• Operate, maintain, and troubleshoot laboratory instruments.
• Review, interpret, and report patient results using LIMS.
• Identify and resolve complex issues impacting test performance.
• Conduct, review, and document laboratory quality control processes.
• Document corrective measures when testing systems deviate from set performance standards.
• Perform and log routine preventive maintenance.
• Prepare necessary reagents for testing procedures.
• Conduct and document reagent qualification.
• Engage in assay enhancements, new assay configurations, and validation efforts.
• Provide direct oversight of unlicensed laboratory staff during analytical testing.
• Communicate effectively with colleagues and non-laboratory personnel.
• Process specimens, conduct tests, report results, and maintain patient testing records.
• Administer proficiency testing samples in the same manner as patient specimens.
• Follow quality control protocols and document quality control, calibration, and maintenance activities.
• Identify, rectify, or report issues affecting test performance or result accuracy.
• Report any quality and safety concerns regarding tests to laboratory leadership.
• Critically assess and responsibly utilize AI-enabled tools in line with company policies, ethical standards, and regulatory requirements.
• Must hold a current, valid CLS or Clinical Genetic Molecular Biologist Scientist (CGMBS) license issued by the state of California, or an appropriate physician, osteopathy, or podiatry license for the relevant specialties.
• Must meet the standards outlined in 42 CFR 493.1489 or 493.1491.
• Must satisfy the criteria described in 10 NYCRR Part 58-1.5.
• Must adhere to the requirements set forth in the College of American Pathologists Molecular Pathology Checklist.
• A Bachelor's degree or equivalent in Biomedical Laboratory Science, Clinical Science, or a related field is preferred.
• Experience in Guardant Health Clinical Laboratory or equivalent high complexity and volume laboratory setting is preferred.
• Laboratory experience within the past year is preferred.
• Familiarity with molecular biology techniques is preferred.
• Knowledge of local, state, and federal laboratory regulations is preferred.
• Ability to incorporate and apply feedback in a professional context.
• Capability to manage daily testing operations with a strong emphasis on quality.
• Proficient in analyzing and solving basic issues that influence test performance.
• Ability to collaborate effectively as part of a team.
• Strong computer and automation skills are essential.
• Must be able to communicate proactively, consistently, clearly, and honestly.
• Must be capable of meeting the demands of the work environment, including prolonged standing or sitting, repetitive manual pipetting, and lifting up to 25 pounds.
• Background screening, including a criminal history check, is required.
• Hybrid work model offering work-from-home days for eligible onsite employees.
• Reasonable accommodations available for disabilities, long-term conditions, mental health conditions, and sincerely held religious beliefs.
• Commitment to equal opportunity employment.
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