Technical Specialist-High Complexity Lab - Lovelace Division, (1312)

Scheduled Shift Monday-Friday 8-5 with holidays, occasional weekends, and other shifts as needed. Location Lovelace Division Job Summary Provides technical expertise for the technical performance for assigned area or discipline(s). Responsible for Quality Control, proficiency and developing competency testing. Offers critical technical recommendations regarding decisions on matters relating to patient care, technical performance, quality and cost analysis. May perform the responsibilities of a Technical Supervisor under Code of Federal Regulations (CFR) 493.1451 except in the specialties of clinical Cytogenetics, Cytology, Histocompatibility, Histopathology and Transfusion Medicine. Essential Functions Serves as a technical resource for all testing sites in area or discipline(s). Provides moderate to complex technical assistance in the development of new assays or procedures. Interprets data and makes recommendations to the relevant supervisor, manager, or pathologist/medical director. Researches and resolves problems and/or provides guidance and counsel to others in resolving problems appropriately. Consults with and makes recommendations to supervisor, manager, or pathologist/medical director regarding difficult analyses, abnormal findings or conflicting results. Ensures maintenance, review of records and recommendations for upgrades for instruments are performed. Participates in developing and implementing computer system improvements for computer systems that include existing systems, middleware and new systems. Works with Information Technology department to ensure computer file maintenance for relevant assays is correct and up to date. Develops new procedures and special reports as needed. Successfully performs appropriate tests in the section as required based on company need. Actively participates in the technical workgroup and communication of changes. Performs cost accounting exercises for testing. Responsible for Quality Control (QC) for assigned section. Reviews monthly QC reports, summarizes data, monitors for trends, looks for problems, makes recommendations to management and/or Pathologist or their designee based on results of analysis. Leads and/or participates in quality initiatives for section assuring compliance with the provisions of regulatory agencies. Recommends, develops, monitors and reports on Quality Assurance (QA) standards and objectives. Serves as a resource and advisor for QA/QC problem situations; works to resolve situations as they occur. Facilitates and/or participates in Quality Management Teams. Researches, develops, implements, maintains and documents standard laboratory procedures. Ensures department/section compliance with all regulatory agencies and inspections. Participates in on-site inspections by regulatory agencies. Researches and interprets regulations to help ensure laboratory remains in compliance at all times. Designs, implements and assesses employee and/or student training and/or competency testing. Designs, implements and ensures proficiency testing is performed as scheduled, results are evaluated, and any required corrective (technical) action is performed. Provides input to staff performance if requested. Minimum Education Bachelor Degree in a relevant field. Minimum Experience Four (4) years of clinical lab experience. Other Requirements ASCP Technologist/Scientist certification or equivalent. Preferences Specialty certification and/or training if available. The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified. #J-18808-Ljbffr TriCore Reference Laboratories