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Senior Clinical Laboratory Scientist - Am Shift #2969
Company | GRAIL |
Address | Menlo Park, CA, United States |
Employment type | FULL_TIME |
Salary | |
Category | IT Services and IT Consulting,Software Development,Biotechnology Research |
Expires | 2023-06-23 |
Posted at | 1 year ago |
GRAIL is a healthcare company whose mission is to detect cancer early, when it can be cured. GRAIL is focused on alleviating the global burden of cancer by developing pioneering technology to detect and identify multiple deadly cancer types early. The company is using the power of next-generation sequencing, population-scale clinical studies, and state-of-the-art computer science and data science to enhance the scientific understanding of cancer biology, and to develop its multi-cancer early detection blood test. GRAIL is headquartered in Menlo Park, CA with locations in Washington, D.C., North Carolina, and the United Kingdom. GRAIL, LLC is a wholly-owned subsidiary of Illumina, Inc. (NASDAQ:ILMN). For more information, please visit www.grail.com .
- Independently identify and troubleshoot high complexity problems that adversely affect the test performance.
- Identify process improvement opportunities and report to laboratory management.
- Write and revise standard operating procedures, as needed.
- Operate and maintain laboratory instruments and equipment according to laboratory standard operating procedures Troubleshoot and problem solve instrument issues. Check, monitor and record temperature and perform root cause analysis of deviations and implement a resolution or initiate a service request as necessary.
- Perform other laboratory duties as assigned.
- Document all corrective actions taken when test systems deviate from the laboratory’s established performance specifications.
- Participate in cross-functional teams responsible for securing CLIA certification, CAP accreditation, and state licensure for the GRAIL Clinical Laboratory, including compliance with all applicable standards and regulations.
- Perform and document reagent qualifications per the approved protocols.
- Provide direct supervision of the work of unlicensed laboratory personnel during the analytical phase of testing.
- Perform, review and document laboratory quality control procedures.
- Participate in introduction of assay improvements, new assay configurations and validation.
- Lead in introduction of assay improvements, new assay configurations and validation. May act as a team leader, when assigned, who will provide assistance to the Laboratory Supervisors/Leads Assist in administrative duties including but not limited to review of documents and forms.
- Monitoring data and process status as needed
- Review, interpret and report patient results as assigned.
- Assist in sample and process troubleshooting
- Communicate effectively with coworkers and non-laboratory personnel.
- Perform and document routine preventive maintenance.
- Assist with training of new laboratory personnel and training of new procedures with existing personnel.
- Perform analytical procedures including testing, quality control, preparation and aliquoting of reagents and analyses according to the laboratory’s standard operating procedures.
- Report all concerns of test quality and/or safety to the Laboratory Manager or Safety Officer.
- Take charge of shift communication if supervisors/leads are not presentProvide updates to supervisors/lead regarding any issues
- Participate and comply with Quality and applicable regulatory requirements.
- Bachelor of Arts or Science in Biomedical Laboratory Science, Clinical Science or related field
- Strong automation and computing skills
- Laboratory testing experience within the last five years preferred
- Must possess a valid California Clinical Laboratory Scientist license
- Working knowledge of local, state, and federal laboratory regulations
- High volume laboratory experience preferredExperience in molecular biology techniques preferred
- Ability to prioritize tasks with a high emphasis on qualityAbility to proactively communicate consistently, clearly, and honestly
- Flexibility of work schedule to meet the needs of GRAIL’s Clinical Laboratory
- At least 4-6 years of Clinical Laboratory experience or equivalentAble to integrate and apply feedback in a professional manner
- Ability to work as part of a team in a highly collaborative environment
- Ability to analyze and problem solve complex issues that may impact test performance
- Strong technical skills and job and industry knowledge
- Able to prioritize and drive to results with a high emphasis on quality
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