Larina Oliveira has extensive experience in the pharmaceutical industry, currently serving as an Analista Pleno for Regulatory Affairs at Hypera since August 2016, focusing on the qualification of Active Pharmaceutical Ingredients (API) and Drug Master Files (DMF). Previous roles at Hypera include positions in Quality Assurance, where responsibilities encompassed supplier qualification and thorough evaluation of production processes. Before joining Hypera, Larina worked as a Junior Quality Assurance Analyst at Greenpharma, engaging in compliance with Good Manufacturing Practices (GMP), deviation investigations, and internal training. Early career experience includes a quality control internship at Industria Farmaceutica Melcon do Brasil Ltda. Larina holds an MBA in Pharmaceutical Industrial Management from IPOG and a Bachelor's degree in Pharmacy from Universidade Estadual de Goiás.
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