Jennifer Johnson, Process Development Scientist
Jennifer brings to Arete over ten years of experience with in vitro diagnostic (IVD) product development and regulatory compliance. In both laboratory and management roles, she has followed products from R&D concept to regulatory submission within quality management systems and design control processes including technical feasibility, verification and validation, drafting of regulatory submissions, and transfer of products to manufacturing. Jennifer’s focus areas have included monoclonal antibody and immunoassay development, molecular diagnostic assay development, assay integration with consumables and instrumentation, technical writing, and GLP compliance. She holds a BS in Plant Biology and an MS in Environmental Studies, both from Ohio University, as well as a Global Health Delivery certificate from Harvard University.