Molecular Technologist II

Summary of Position Under general supervision, responsible for performing and reporting high-throughput, clinical genotyping assays using molecular platforms, operating and maintaining laboratory equipment needed to perform daily duties; increasing productivity and maintaining proficiency in the wet lab and analysis sections; adhering to laboratory policies for safety, conduct, and performance. Key Job Elements Extract and quantify DNA and RNA from blood and tissue samples. Perform PCR reactions. Perform specified assays for genotyping services in accordance with the SOP. Prepare and evaluate test results for completeness, accuracy, and quality. Report test results in LIS. Receive, unpack, log customer samples according to SOPs. Perform troubleshooting, maintenance, and calibration of instrumentation and equipment used to conduct testing in compliance with quality control/assessment standards. Participate in the development and/or maintenance of SOPs as required. Identify ways in which laboratory procedures and activities can be modified to improve upon current methodologies. Optimize diagnostic tests and update existing standard operating protocols with significant guidance. Work with laboratory supervisor for troubleshooting and determine solution. Participate in lab meetings and generate ideas for improving efficiency and productivity in the daily operation of the lab. Comply with all aspects of laboratory safety, safety stations, safety manuals, safety SOP, and MSDS sheets. Leadership: Assist with assigned additional duties in a specialized area of the laboratory. Qualifications BS in biological science or equivalent with three (3) or more years of training/experience in a clinical molecular laboratory. MB (ASCP) Certification – Current. Laboratory personnel participating in licensure or certification maintenance programs must complete the number of continuing education prescribed by the licensing or certifying agency. Technical laboratory personnel whose certification has been grandfathered and does not require participation in a certification maintenance program must complete at least twelve hours of continuing education annually. Lab experience and/or training in a clinical laboratory setting. Preferred experience in molecular pathology. Must satisfy requirements for high complexity testing under CLIA regulations (42 CFR, part 493). Superior communication (written and verbal), time management and organizational skills. Working Conditions Exposure to biological hazards associated with human specimens. Standard universal precautions required for handling specimens. Equal Opportunity Statement Fulgent Therapeutics LLC is an Equal Employment Opportunity Employer. Work Environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. The term “qualified individual with a disability” means an individual with a disability who, with or without reasonable accommodation, can perform the essential functions of the position. #J-18808-Ljbffr