Responsibilities - Supports the execution of regulatory planning and operational activities across LATAM for Electrophysiology (EP) and Neurovascular (NV) portfolios - Supports dossier delivery to Local Operating Companies (LoCs) - Contributes to data-driven decision-making and drives process standardization to enable efficient lifecycle management (LCM) and new product introductions (NPI) - Executes the preparation and delivery of regulatory dossiers to LoCs ensuring completeness and compliance with local requirements - Tracks dossier submission timelines and ensures alignment with regulatory action plans and market needs - Supports document management activities,



including version control - Acts as a liaison between regional teams and LoCs to ensure clarity on dossier requirements - Contributes to planning and forecasting activities - Maintains regional trackers, dashboards, and planning tools - Consolidates and analyzes regulatory performance metrics - Identifies opportunities to improve planning, dossier delivery, and operational processes Requirements - Bachelor’s degree in Pharmacy, Engineering, Life Sciences, or related field - 0–2 years of experience in Regulatory Affairs or related field - Strong analytical and problem‑solving skills - High attention to detail and process orientation - Proficiency in Excel; data visualization tools (e.g., Power BI) is a plus - Advanced or intermediate skills in English/ Spanish is preferred.

📌 Regulatory Affairs Analyst (Lima)
🏢 Jobtailor
📍 Lima