Erika Gallardo is an experienced professional in the chemical engineering and regulatory affairs sectors. Currently serving as Jefe de Produccion API at SYNTEX S.A, Erika oversees the production of injectable heparin and chondroitin sulfate, ensuring compliance with GMP standards. Previously, as an Analista de Asuntos Regulatorios at both SYNTEX S.A and Estudio Levy Guido & Levy, Erika managed the registration of veterinary and cosmetic products with authorities such as SENASA and ANMAT. Erika's academic achievements include a degree in Chemical Engineering from the University of Buenos Aires and additional qualifications in Cosmetic Chemistry and Industrial Pharmacy.
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