Histogen
Jessie A. is a seasoned professional with extensive experience in quality management and regulatory compliance within the clinical and biotech sectors. Currently serving as Director of Quality at Histogen, Jessie leads a Quality team focused on team-building and quality management system development. Previously held positions include Manager of Quality & Regulatory at CSL Behring, where compliance and patient safety were prioritized, and roles at Biocept, Immucor, Abbott, and U.S. Laboratories, emphasizing leadership in quality operations, product development, and regulatory adherence. Jessie holds a B.S. in Medical Technology from the University of Pangasinan and an MBA in International Business from Florida Metropolitan University, alongside education from Harvard Medical School and Scilife in Madrid. Key skills include expertise in filtration techniques, product optimization, and compliance with regulatory frameworks such as FDA and CLIA.
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Histogen
Histogen is a clinical-stage therapeutics company focused on developing potential first-in-class restorative therapeutics that ignite the body’s natural process to repair and maintain healthy biological function. Histogen’s innovative technology platform utilizes cell conditioned media and extracellular matrix materials produced by hypoxia-induced multipotent cells. Histogen’s proprietary, reproducible manufacturing process provides targeted solutions across a broad range of therapeutic indications including hair growth, dermal rejuvenation, joint cartilage regeneration and spinal disk repair.