Silvia Ruggieri is a Clinical Scientist at Meditrial since March 2022, specializing in regulatory and clinical development strategies within the cardiovascular and gastrointestinal sectors, including trial design and FDA submissions. Previously, Silvia held the position of Quality Engineer at Linkverse, focusing on medical device compliance and technical documentation, from August 2020 to March 2022. As a Medical Device and CSV Consultant at PQE Group from October 2018 to August 2020, Silvia advised on quality and regulatory matters, including ISO standards and risk management. Silvia began their career at Cnim S.r.l. as a QMS Auditor, where responsibilities included QMS verification and audit preparation, and also served as a QMS Technical Officer, supporting the QA manager with SOPs and quality documentation. Silvia's experience includes an internship as a System Management Consultant, with a strong educational background comprising a Master's Degree in Biomedical Engineering and a Bachelor's Degree in Clinical Engineering from Sapienza Università di Roma.
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