GMP Compliance Advisor & Auditor @PQE Group - Stefania has been a project leader for different biotechnological products development, from engineering up to process validation and she has been responsible for a part of the development and production activities for more than 7 years.
She has a long and strong experience working in pharma industries, from producing proteins involved in cancer development to developing processes and analytical methods for monoclonal antibodies to be used as orphan drugs. Reinforced by her Biotechnology degree and Master in Preclinical and Clinical Drugs Development, her wide knowledge include Quality Assurance, Toxicology, Clinical trials, drugs’ market, GMP regulated environments, as well as products compliance with EMA and FDA requirements.
