Cyro Idalgo
Senior Analytical Chemist @Dalton Pharma Services
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WORK HISTORY
Senior Analytical Chemist @Dalton Pharma Services
North York, ON, CA
Leading analytical assessments with a “right-first-time” mindset in a GMP and FDA-compliant facility. • Performed method development and method validation according to FDA and ICH Q2 standards. • Drafted and executed analytical validation protocols and comprehensive reports. • Contributed to continuous process improvement and troubleshooting during method development. • Technologies used: HPLC, UPLC, CAD, DAD, ELSD, GC, Elemental Analyzer, ChemStation, OpenLab.
EDUCATION
Universidade Guarulhos
Bachelor's degree, Chemistry
Universidade Guarulhos
Bachelor's degree, Pharmacist
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
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