In this role, you will supports proper documentation of all elements of CAP accreditation and inspection including the quality management program; chemical hygiene plan; document control process; competency assessment program; and test method validation documentation.
In this role, you will perform routine and specialized procedures, and reviews and approves clinical test results, for use in diagnosis and treatment of patients, in accordance with established protocol for laboratory performing high complexity procedures as defined by standards of Clinical Laboratory Improvement Amendments of 1988 (CLIA 88).
In this role, you will be responsible to Create and maintain individual training folder in accordance with laboratory standards. Understand and assist in the performance and testing requirements associated with FDA regulated testing; and be prepared to execute testing in accordance with SOPs.
In this role, the selected candidate must be able to ensure that critical and delta values are strictly handled according to policy. Perform quality control, daily maintenance and document records and logs as appropriate.