Clinical Laboratory Scientist II, Reporting
About the position
The Clinical Laboratory Scientist (CLS) II is responsible for performing high complexity laboratory testing on patient specimens, performing quality control and quality assurance procedures, and complying with all applicable local, state and federal laboratory requirements. The 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 in a team environment.
Responsibilities
• Perform laboratory tests, procedures and analyses according to the laboratory’s standard operating procedures
• Operate, maintain and troubleshoot equipment according to the laboratory’s standard operating procedures
• Review, interpret, and report patient results in LIMS as assigned
• 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 established performance specifications
• Perform and document routine preventive maintenance
• Prepare reagents required for testing
• Perform and document reagent qualification per the approved protocols
• Participate in introduction of assay improvements, new assay configurations and validation
• Provide direct supervision of the work of unlicensed laboratory personnel during the analytical phase of testing
• Write and review of controlled documents as assigned
• Assist with the training of new and existing laboratory personnel on current and new procedures
• Communicate effectively with coworkers and non-laboratory personnel
• Perform other laboratory duties as assigned
• Report all concerns of test quality and/or safety to the Laboratory Supervisor, Laboratory Director or Safety Officer
Requirements
• Must possess an active, valid CLS or Clinical Genetic Molecular Biologist Scientist (CGMBS) license issued by the state of California CLS or CGMBS license pursuant to Division 2, Chapter 3 of the California Business and Professions Code or to practice medicine, osteopathy or podiatry pursuant to Division 2, Chapter 5 of the California Business and Professions Code appropriate to the specialty or specialties they are performing
• Must fulfill requirements stated in 42 CFR 493.1489 or 493.1491
• Must fulfill requirements stated as described in 10 NYYCRR Part 58-1.5
• Must fulfill requirements stated in the College of American Pathologists Molecular Pathology Checklist
• Strong computer and automation skills
• Ability to proactively communicate consistently, clearly, and honestly
Nice-to-haves
• Bachelor’s degree or equivalent in Biomedical Laboratory Science, Clinical Science or related field preferred
• At least one year of Guardant Health Clinical Laboratory experience or equivalent high complexity and volume laboratory experience preferred
• Laboratory experience within the last year preferred
• Experience in molecular biology techniques preferred
• Working knowledge of local, state, and federal laboratory regulations preferred
• Able to integrate and apply feedback in a professional manner
• Ability to manage daily test processing needs with high emphasis on quality
• Ability to analyze and problem solve basic issues that impact test performance
• Ability to work as part of a team
Benefits
• 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.
The Clinical Laboratory Scientist (CLS) II is responsible for performing high complexity laboratory testing on patient specimens, performing quality control and quality assurance procedures, and complying with all applicable local, state and federal laboratory requirements. The 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 in a team environment.
Responsibilities
• Perform laboratory tests, procedures and analyses according to the laboratory’s standard operating procedures
• Operate, maintain and troubleshoot equipment according to the laboratory’s standard operating procedures
• Review, interpret, and report patient results in LIMS as assigned
• 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 established performance specifications
• Perform and document routine preventive maintenance
• Prepare reagents required for testing
• Perform and document reagent qualification per the approved protocols
• Participate in introduction of assay improvements, new assay configurations and validation
• Provide direct supervision of the work of unlicensed laboratory personnel during the analytical phase of testing
• Write and review of controlled documents as assigned
• Assist with the training of new and existing laboratory personnel on current and new procedures
• Communicate effectively with coworkers and non-laboratory personnel
• Perform other laboratory duties as assigned
• Report all concerns of test quality and/or safety to the Laboratory Supervisor, Laboratory Director or Safety Officer
Requirements
• Must possess an active, valid CLS or Clinical Genetic Molecular Biologist Scientist (CGMBS) license issued by the state of California CLS or CGMBS license pursuant to Division 2, Chapter 3 of the California Business and Professions Code or to practice medicine, osteopathy or podiatry pursuant to Division 2, Chapter 5 of the California Business and Professions Code appropriate to the specialty or specialties they are performing
• Must fulfill requirements stated in 42 CFR 493.1489 or 493.1491
• Must fulfill requirements stated as described in 10 NYYCRR Part 58-1.5
• Must fulfill requirements stated in the College of American Pathologists Molecular Pathology Checklist
• Strong computer and automation skills
• Ability to proactively communicate consistently, clearly, and honestly
Nice-to-haves
• Bachelor’s degree or equivalent in Biomedical Laboratory Science, Clinical Science or related field preferred
• At least one year of Guardant Health Clinical Laboratory experience or equivalent high complexity and volume laboratory experience preferred
• Laboratory experience within the last year preferred
• Experience in molecular biology techniques preferred
• Working knowledge of local, state, and federal laboratory regulations preferred
• Able to integrate and apply feedback in a professional manner
• Ability to manage daily test processing needs with high emphasis on quality
• Ability to analyze and problem solve basic issues that impact test performance
• Ability to work as part of a team
Benefits
• 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.