Laboratory Technologist I or II - 3rd shift

Responsibilities

Position Summary

This position is responsible for specimen processing, test performance (one or more donor screening platforms), and reporting test results in a high complexity laboratory serving multiple internal and external clients. This laboratory performs infectious disease and immunohematology testing relevant to blood and HCT/P donor screening as required by the FDA and New York State Department of Health. Primary Duties: Specimen Processing (Pre-analytic): Receive, label, and prepare samples for testing; ensuring proper handling and storage. Prepare and pack samples for send-out testing according to IATA shipping requirements. Perform Donor Screening Testing (Analytic): Performs testing and interprets data to generate test results on one or more donor screening platforms (serologic testing for viral markers, immunohematology, Nucleic Acid Testing (NAT/PCR), or additional viral screening assays), utilizes multiple laboratory information systems, and operates a variety of lab equipment according to established policies and procedures and reports results accordingly. This position performs only those tests that are authorized by the CLIA/NYSDOH laboratory director and performs only those tests that require a degree of skill commensurate with the individual's education, training or experience, and technical abilities. Data Analysis (Post-Analytic): Performs primary record review of test records. Performs secondary record review once trained and competent, as assigned by supervisor. Documentation and Reporting: Ensures adherence to Good Documentation Practices by accurately documenting on all test records. Critical Thinking and Problem Solving: Recognizes and reports to department leadership problems encountered during performance of job tasks including unusual test results, discrepancy in test controls, or controls outside established normal limits. Documents Failed Runs, as applicable. Equipment Troubleshooting: Performs troubleshooting steps for equipment malfunctions. Follows equipment out of service procedure and documents corrective actions taken when test systems deviate from the established performance specifications. Error Management: Documents when deviations from standard operating procedures (SOPs) are discovered. Assists with investigations and complies with corrective/preventative actions implemented. Inventory Management: Performs and documents inventory receipt procedures for test reagents and supplies according to established policies and procedures. Monitors and maintains adequate laboratory supplies. Quality Control: Performs and documents quality control procedures for test reagents (reagent prequalification) according to established policies and procedures. Maintains strict adherence to Good Manufacturing Practices, ensuring meticulous attention to detail in all processes. Equipment Maintenance: Performs and documents routine maintenance/calibration activities for all laboratory equipment on which the individual is currently trained. Follows laboratory policies and procedures whenever test systems are not within the laboratory’s established performance specifications. Regulatory Compliance: Complies with all established policies and procedures including testing and reporting protocols, safety practices, donor and patient confidentiality policies, and personnel practices. Safety and Sanitation: Promotes and contributes to a culture of safety through compliance with all safety SOPs to include wearing proper personal protective equipment (PPE) I.e. safety shields/goggles, gloves, lab coats and proper shoes. Promptly report all safety violation observations and/or safety concerns. Assures a clean and orderly work area including maintenance and efficient use of reagents, supplies and stored samples. Customer Service: Provides excellent customer service to both external and internal customers. Promotes teamwork and communication both internally and externally. Secondary Functions: Additional Regulatory Compliance: Satisfactorily performs assigned proficiency testing in the same manner as donor samples and always follows Good Manufacturing Processes, with attention to detail. Successful completes annual competency assessment programs and annual organizational training. Continuous Improvement: Complete required continuing education credits to meet national or state regulatory requirements Research and Clinical Trials: Participates in clinical trials and/or investigational studies of reagents, equipment, or new test methods.