Under the minimal supervision of the SCID-SMA Screening Group Manager, this role plans, directs, and manages the technical resources and activities of the SCID-SMA Newborn Screening Team. The position ensures analytic accuracy is maintained and process corrections are implemented by utilizing expert working knowledge of all procedures. It involves developing, establishing, and updating standard protocols for the molecular testing of Severe Combined Immunodeficiency (SCID) and Spinal Muscular Atrophy (SMA) using real-time polymerase chain reaction (RT-PCR) and other procedures. The role monitors and documents quality assurance issues, including specimen turnaround time, quality control, quality assurance, and proficiency testing performance. It is responsible for making significant decisions about the accuracy of laboratory tests on human specimens, participating in personnel training, and encouraging communication within the team. The position also assists in preparing laboratory budgets, providing cost analysis, assessing equipment needs, and incorporating new technologies. It provides information to public health personnel and serves as an authority, technical resource, and positive role model. Duties are performed with extensive latitude to develop and interpret protocols with advanced use of scientific knowledge and judgment. The role supports the creation of a laboratory-wide safety culture by serving as a liaison to the Safety Office to ensure a healthy and safe workplace. Work hours/days and laboratory assignments may vary, and all staff members will be required to work on Saturday as part of a rotating schedule.
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Job Type
Full-time
Career Level
Senior