Mário Silvério is a Specialist in Quality Compliance at BioNTech SE since August 2022, focusing on GCP for labs, CAP/CLIA, and GxP Compliance within the BioX Biosampling Unit. Prior experience includes a role as MS&T Engineer at VTU Engineering for manufacturing support and as Clinical Trial Associate and Laboratory Supervisor at Profil, managing clinical laboratory operations and overseeing the conduct of biological sample processing under GCLP standards. Mário also contributed to the Pharma Supply Chain Risk Management project at House of Logistics and Mobility (HOLM) GmbH, and served as a Research Associate at Hochschule RheinMain, developing web-based software solutions for pharmaceutical logistics. Additionally, Mário held a Scientific Research Assistant position at Universidade de Coimbra, focusing on molecular mechanisms of disease. Educational background includes a Bachelor of Science in Biotechnology from Politécnico de Coimbra.
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