Alessandro Lobbia

Alessandro Lobbia has extensive experience in regulatory affairs and quality assurance in the pharmaceutical industry. Alessandro is currently serving as the Vice President of Regulatory CMC at Pacira BioSciences, Inc., where they oversee the department's activities and leads the preparation of regulatory documents and filings. Prior to this, they worked at Neurocrine Biosciences as the Executive Director of Regulatory CMC, where they developed and implemented regulatory strategies for company projects. Alessandro also served as the Senior Director and Head of Regulatory Affairs and Quality Assurance at Tocagen Inc., where they led the regulatory and quality assurance departments. Alessandro has also worked as an independent consultant, as well as in various roles at Cadence Pharmaceuticals, Favrille, Biogen Idec, IDEC Pharmaceuticals, and Schering AG, gaining experience in regulatory leadership, team management, and regulatory document review and organization.

Alessandro Lobbia attended the Università degli Studi di Padova from 1974 to 1979, where they pursued a degree in Dottore in Chimica (Doctor of Chemistry). Alessandro'sfocus of study during this time was Chemistry.