Tiago Capozzi is an experienced professional in analytical development and validation with a career spanning over a decade in the pharmaceutical industry. Currently serving as an Analytical Development and Stability Consultant at PQE Group since May 2023, Tiago has a strong background in developing and validating analytical methods in compliance with RDC regulations. Previous roles include positions at EMS and Catalent Pharma Solutions Brasil, where responsibilities encompassed analytical method development and validation. Additional expertise includes supervisory and consulting roles at various pharmaceutical companies, focusing on analytical methods for product characterization and stability analysis using techniques such as chromatography and spectrophotometry. Tiago holds a degree in Pharmacy/Biochemistry from Universidade Paulista, completed in 2011.
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