Under the minimal supervision of the Newborn DNA Analysis Group Manager, plans, directs, and manages the technical resources and activities of the Newborn DNA Analysis Team. Utilizes expert working knowledge of all procedures to ensure that analytic accuracy is maintained and process corrections are implemented. Uses expert knowledge to develop, establish and update standard protocols for the molecular testing of relevant human genetic diseases including cystic fibrosis, sickle cell disease, medium chain acyl-CoA dehydrogenase deficiency, galactosemia, X-linked adrenoleukodystrophy, very long chain acyl-CoA dehydrogenase deficiency (VLCAD), spinal muscular atrophy, and other NBS disorders by identification of mutations using PCR, DNA sequencing, and other related procedures. Monitors and documents quality assurance issues including specimen turnaround time, quality control, quality assurance, and proficiency testing performance. Responsible for making significant decisions about the accuracy of laboratory tests on human specimens. Participates in the training of personnel on the team and encourages communication within the team. Participates in preparing laboratory budgets, providing cost analysis, assessing equipment needs and incorporating new technologies. Provides information to public health personnel. 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. Supports the creation of a laboratory-wide safety culture to ensure a healthy and safe workplace. Work hours/days and laboratory assignments may vary, 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
Mid Level
Number of Employees
1-10 employees