Pharmacovigilance professional with 5+ years of experience in safety operations, clinical research, and quality systems within leading pharmaceutical organizations. Expertise in ICSR intake and processing, MedDRA coding, causality assessment, and global case management. Strong contributor to process excellence through SOP/WI development, workflow optimization, and cross-functional collaboration. AI-driven and automation-oriented, with experience implementing Python-based tools and machine-learning approaches to improve efficiency, accuracy, and compliance. Polyglot communicator (SP/EN/FR/PT) with a solid scientific background, hands-on research experience, and ongoing specialization in Machine Learning—bridging pharmacovigilance expertise with data-driven innovation in regulated environments.