PROFESSIONAL STATEMENT Responsible of Regulatory Dept. at Cloverty (head office & CDMO), accountable for Pharma and Food Supplements (FS). Activities in charge include Preparation of Registration Dossiers, Documentary + Regulatory Support, Interaction with Authorities & Customers, etc. Currently leading a team of 3 technicians providing support to +50 clients in +100 countries.Formation in Registration and Regulatory (MSc), Clinical Research and Scientific background in R&D in Pharma (GlaxoSmithKline, +10 years) with experience as Project Leader in Int’l programs.My professional objective is to progress my technical career in Regulatory, specializing in Novel Projects, Regulatory Intelligence, MAA and Cross-National Registration strategies.I provide initiative, commitment and autonomous management. KEY STRENGTHS• Excellent organizational and planning skills.• Matrix Leadership. Team Player. Accomplished communicator.• Entrepreneur – Innovative, challenging solutions: Technical / Scientific • Committed and Enthusiastic for learning. Problem solving attitude.