Cyro Idalgo

Background

About Cyro Idalgo

Experienced Analytical Chemist with 10+ years in GMP-regulated pharmaceutical and chemical industries, specializing in analytical method validation, stability studies, method development and quality control. Extensive expertise in HPLC, UPLC, GC, dissolution, and impurity profiling, using systems such as Empower 3, ChemStation, and OpenLab. Proven track record of successful compliance with FDA and EMA guidelines, including ICH and EU GMP standards. Strong knowledge of regulatory documentation, deviation investigations (OoS, OoT), and cross-functional collaboration in international environments. Experienced in analytical development, method transfer, and project leadership. Native Portuguese speaker with fluent English. Open to remote collaboration and global projects, particularly across Canada and Europe. Areas of expertise: • Analytical Method Validation (FDA, EMA, ICH Q2) • HPLC, UPLC, GC, CAD, ELSD, DAD, RI • Stability Studies (Photostability, Hold Time, ICH Guidelines) • Dissolution, Assay, Impurities, RS • GMP, Quality Control & Analytical Development • Regulatory Compliance & Documentation • Empower, ChemStation, OpenLab, LIMS, SAP • Team Leadership & Process Optimization