Life Sciences professional with over 15 years of experience in multinational pharmaceutical companies. Strong background in Regulatory Compliance, Risk Management, Product Lifecycle Management, Product Safety, and KPI-driven project timelines. Extensive experience navigating Brazilian legislation for pharmaceutical products, including new drugs, biologics, medical devices, and cosmetics, ensuring compliance with ANVISA, CMED, and INMETRO standards.Skilled in interpreting and applying regulatory laws and guidelines to ensure organizational compliance, Feasibility planning of new products and alterations, acting in management and excecution to achieve KPIs; Regulatory Intelligence for monitor the market and competitors, offering strategic recommendations to enhance business/ project outcomes. Adept at project management, leading cross-functional teams to meet key milestones, and tracking KPIs for regulatory timelines to maintain alignment with business goals and budgets.Key strengths include:• Regulatory Affairs and Quality Assurance Management – Expertise in GxP compliance, SOPs, Pharmacovigilance, and end-to-end product lifecycle management with a focus on Regulatory Strategy.• Project Management and Timeline Optimization – Experienced in establishing, monitoring, and delivering projects according to KPI-based timelines, ensuring smooth regulatory submissions and successful Marketing Authorization.• Regulatory Strategy Development – In-depth experience with processes, KPIs, and managing strategic submissions aligned with organizational goals.• Problem Solving and Decision-Making – Demonstrated ability to navigate complex regulatory landscapes, applying data-driven insights to support strategic objectives.• Self-Motivation and Adaptability – Known for thriving in dynamic environments, with a consistent focus on achieving compliance, quality, and project milestones.• Self-managing.• Active CRF.