Carlos has over fifteen (15) years of experience in the pharmaceutical industry. He has extensive experience in Pharmaceutical Development and Regulatory Compliance. In the past, he successfully applied QbD principles in drug product and drug substances development and drove drug products through development, clinical and regulatory approval. He also has experience in GCP compliance and Quality Assurance activities. His experience also includes team management and technical leadership in partnership projects with companies in Canada, USA and Europe.
He holds a B.Sc. in Pharmacy from UNMSM, Peru; a MSc in Pharmaceutical Industry from IPIL (University of Lyon 1) / EMLYON, France; and a certificate in Project Management from the HEC Montreal, Canada.