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.