Provide day-to-day supervision of testing personnel and reporting of test results within the high complexity Clinical Testing Laboratory
Coordinate the activities of junior team members to ensure the completion of clinical testing within agreed timeframes
Monitor specimen examinations and test analyses to ensure that acceptable levels of analytic performance are maintained at all times.
Responsible for the generation, revision, and/or review of laboratory or equipment-related SOPs and other quality documents
Perform molecular biological techniques adhering to the laboratory's quality control policies.
Ensure that all remedial actions are taken in a timely manner whenever test systems deviate from the laboratory's established performance specifications and leadership is notified as required.
Be accessible to testing personnel at all times testing is performed to provide on-site, telephone or electronic consultation to resolve technical problems in accordance with policies and procedures.
Monitor batch manufacturing stock levels and coordinate ordering and testing of new reagent and control batches to ensure adequate supply for clinical testing. Verify reagents, consumables, and laboratory equipment are qualified for use and within expiry.
B.S. in chemical, biological, medical, clinical laboratory science, or medical technology from an accredited institution
B.S. or MS degree, with 4+ years of training/experience in at least one of the following technologies: qPCR, Nanostring, and/or NGS, OR
Ph.D., with 1+ year of training/experience in at least one of the following technologies: qPCR, Nanostring, and/or NGS
M.S. in chemical, biological, medical, clinical laboratory science, or medical technology from an accredited institution or Ph.D. in chemical, biological, medical, clinical laboratory science, or medical technology from an accredited institution
ASCP Board Certification as a Specialist in Molecular Biology
Excellent oral and written communication skills
Attention to detail
Experience in a high complexity CLIA testing environment
Experience with data analysis and reporting of results in at least one of the following technologies: qPCR, Nanostring, and/or NGS
Substantial experience in troubleshooting molecular laboratory techniques
Experience preparing for/participating in laboratory audits, from CAP and other regulatory agencies
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