Emanuele Volpe

Emanuele Volpe possesses extensive experience in pharmaceutical quality systems, currently serving as a GMP Compliance Advisor and Auditor at Pharma Quality Europe since August 2012, where responsibilities include the development and review of Quality Management Plans, compliance assessments for FDA and EU regulations, and management of non-conformances and deviations. With a strong background in project management across various methodologies, Emanuele effectively collaborates with cross-functional teams and key stakeholders to ensure the success of quality initiatives. Previous roles at Novartis involved quality assurance in aseptic operations and vaccines manufacturing, while academic achievements include a Master's in Quality and Environmental Management and a degree in Medical Biotechnology from Sapienza Università di Roma.