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Marzia Paternicò has extensive work experience in quality assurance and regulatory affairs in the pharmaceutical and medical device industries. Marzia began their career at Hammer Pharma S.p.A. in 2004 as an R&D professional before moving to Naturex as a Regulatory Affairs Manager in 2007. In 2011, they joined Biopharmitalia S.p.A as a Quality Assurance Specialist. Marzia then transitioned to Zambon in 2012, where they worked in Compliance and Internal Audit QA. In the same year, they also joined the Helsinn Group as a Corporate Pharmaceutical Technology QA Manager and later became the Manufacturing and CMC Quality Assurance Manager. Currently, Marzia holds the position of Head of Medical Device Quality Assurance & PRRC at the Helsinn Group.

Marzia Paternicò obtained a Laurea magistrale degree in Chemistry from Università degli Studi di Milano.