Benedetta Barro has a strong background in compliance consulting and quality assurance within the pharmaceutical industry. Most recently, they served as a Senior Compliance Consultant, focusing on ensuring regulatory compliance. Prior to that, they worked as a GMP Compliance expert at PQE Group and as a Responsabile assicurazione qualità at OPOCRIN S.P.A. Additionally, Benedetta Barro gained experience as a QA team leader at LDO SpA and as a GMP project specialist and pharmaceutical consultant at JSB Solutions. Benedetta also worked as a Consultant at k2c Compliance Consulting & solutions. Throughout their career, they have been involved in a range of activities, including periodic quality review, qualification and validation activities, quality issues management, and auditing.
Benedetta Barro completed their education in a chronological manner. Benedetta began their education in 2000 at Università degli Studi di Siena, where they obtained a Doctor's degree in pharmaceutical chemistry in 2006. Later, in 2010, they attended Università di Parma and completed a Master's degree in pharmaceutical technologies and regulatory affairs by 2011. Additionally, they briefly studied project management at Alma Graduate School - Bologna in 2012, though it is not mentioned whether they obtained a degree in this field.
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