Wilberto has over fifteen 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. In 2002, Wilberto joined Wyeth as a Microbiology Scientist where he grew and held managerial positions within the microbiology laboratory and in the Compliance Department.
Wilberto also worked in other pharmaceutical companies such as Bristol-Myers Squibb, APP Pharmaceuticals and Blu Pharmaceuticals. In these, he expanded his professional experience in Regulatory Affairs, where he held different leadership positions and took hands-on experience with International, EU, LAC and US regulations; Quality Assurance, where he supported the departmental daily activities and several Regulatory Authority inspections; Validation, where he established and improved different processes and equipment; and in Project Management, where he a lead a companywide project for the implementation of a regulatory electronic submissions system and lead due diligence activities for the acquisition of new manufacturing facilities. 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 Drug Information Association (DIA), 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 Regulatory Affairs, in which he expanded his scope and worked on the registrations of drug products, medical devices and cosmetics in more than 120 countries (mostly in Africa, Asia, and Latin America).