Wilberto Robles, Sr. Director of Global Regulatory Affairs
Wilberto has over sixteen years of professional experience in the pharmaceutical, medical device and cosmetic industry with a special focus in reproductive health products. He holds a Bachelor’s of Science in Microbiology and a Master’s in Manufacturing Competitiveness/Industrial Engineering. … +
Wilberto previous experience includes different positions at Wyeth, Bristol-Myers Squibb, APP Pharmaceuticals and Blu Pharmaceuticals. In these, he focused his professional experience in Regulatory Affairs, where he held different leadership positions working with International, EU, LAC and US registrations; Quality Assurance, Validations, and Project Management. Mr. Robles has publications in the TOPRA International Journal for Professionals in Regulatory Affairs (Regulatory Rapporteur) and the POLITECHNÊ journal and SHPE (The Official Magazine of the Society of Hispanic Professional Engineers). He is an active member of the Regulatory Affairs Professionals Society (RAPS), and The Organization for Professionals in Regulatory Affairs (TOPRA). Mr. Robles is currently working for WCG as the Senior Director of Global Regulatory Affairs, in which he expanded his scope and manage the registrations of drug products and medical devices in more than 120 countries (mostly in Africa, Asia, and Latin America).