•Perform analytical testing for release and stability purpose on APl, excipient, semifinished and finished products;• Perform chemical analysis using chromatographic techniques (HPLC and GC); • Instrumentation for chemical analysis (Dissolution testers, Karl Fisher Titrators, granulometry, pH-meter); • Spectroscopy (IR and UV-Vis) • Ensure that analysis are completed according to established Standard Operating Practices (SOPs), and also Good Laboratory Practices (GLP) or Good Manufacturing Practices (GMP) • Prepare technical documents that report the results of their lab work. • Write testing protocols and trend analyses in a technical reports;• Contribute to laboratory management, such as ordering supplies, organizing maintenance schedules, organizing samples/solvent inventory.

•Developed and validated analytical methods in adherence to EU/US GMP and pharmacopoeia standards;•Wrote and reviewed protocols, reports, and risk assessments following ICH guidelines;•Provided technical support for managing changes and deviations;•Utilized tools such as Tiamo, Empower and Documentum;•Authored and reviewed analytical HPLC methods, SOPs, and WI documents;•Permform analytical testing for validation and analytical transfer purpose; •Perform chemical-physical testing related to complaints;•Offered back-office support during health authority inspections.

Chemical-Physical and Functional Testing for Excipients and Tablets for Direct CompressionExperimental thesis titled: “Chemico-Physical and Technological Characterization of Microcrystalline Cellulose for Direct Compression”