Bruna Brito is a professional with over 10 years of experience in the pharmaceutical industry, specializing in production, quality assurance, regulatory compliance, and quality control. Their expertise encompasses process mapping, deviation investigation, internal auditing, and the implementation of good manufacturing practices (GMP). Bruna has held various roles, including Senior Production Analyst at Baxter International Inc. and has contributed to significant projects aimed at improving process efficiency and compliance. They are currently pursuing a postgraduate specialization in Regulatory Affairs at ICTQ - Instituto de Pós-Graduação para Farmacêuticos.
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