Summary
Marco Carbajal is a Químico Farmacobiólogo with five years of progressive experience in the pharmaceutical sector, specializing in Regulatory Affairs, Technovigilance, and Quality Assurance/Control. He has hands-on expertise ensuring compliance with Mexican NOMs and international standards (GMP, GLP, GDP) and deep knowledge of multiple health and pesticide regulatory frameworks. Marco has worked across analytical labs and regulatory teams, performing physico-chemical analyses, import permit management, audit-trail reviews for data integrity, and COFEPRIS verification support. He combines technical laboratory skills (HPLC, AAS, ICP) with regulatory strategy, helping multinational clients align products and documentation to complex norms. Currently leading regulatory affairs at Adium México, he brings strong organization, root-cause analysis, and cross-functional collaboration to speed compliance and market access. Outside the bench, his GitHub persona "The Sockets Guru" hints at a curious, problem-solving mindset that bridges technical rigor with practical systems thinking.
5 years of coding experience
Químico Farmacobiólogo, Diseño de medicamentos innovadores, Químico Farmacobiólogo, Diseño de medicamentos innovadores at UAM Universidad Autónoma Metropolitana
English