Facilitate training of new technologists.Successfully process specimens for testing, analysis and reporting. Responsible for conducting and documenting all quality control activities, instrument and procedural calibrations, instrument maintenance, and troubleshooting.Create standard operating procedures (SOPs) as required, and research and implement same for state reportable diseases.Accurately maintain patient records, and confidentiality as required by HIPPA.

Use contemporary and novel procedures to perform various analyses on bodily fluids. Perform onsite Micro- ELISA’s., serum enzymatic endpoint and kinetic micro-well chemistries, enzymatic urinalysis, etc., using highly complex analytical procedures, instruments, and/or established manual methods. Review test results for accuracy. Maintain accurate quality control records. Generate patient reports.Participate in proficiency testing and regulatory compliance as necessary.Verify results according to established protocols and enter results into data reduction computer models. Perform and document routine and preventative maintenance on laboratory equipment and instrumentation to assure reliability and accuracy in reporting test results. Perform and document quality control testing. Assist managers in establishing quality control assay values and standard deviations according to established protocols.

•Responsible for generating sales by discovering new clientele • Meeting with prospective business customers to support formulation of new products in their laboratory; and test for efficacy, efficiency, and record results. •Responsible for obtaining updates from our International Distributors •Support International Distributors in promoting Salvona products. • Assessed all orders for proper processing prior to shipment.