Paul Costantini
About Paul Costantini
Paul Costantini is the Director of Global Systems at Bristol Myers Squibb in Summit, New Jersey, with extensive experience in quality systems and risk management within the pharmaceutical industry.
Professional Experience at Bristol Myers Squibb
Paul Costantini currently serves as the Director of Global Systems at Bristol Myers Squibb in Summit, New Jersey, United States. In this role, he has been involved in the implementation and continuous improvement of quality systems since November 2019. He is responsible for the management of electronic document management systems (EDMS) and risk management platforms, specifically utilizing the Veeva Platform. In addition, he oversees deviations, corrective and preventive actions (CAPA), and change control systems using the eTQ platform.
Tenure at Celgene Corporation
Paul Costantini had an extensive career at Celgene Corporation, fulfilling various roles from 2010 to 2019 in Summit, NJ. As Director from 2018 to 2019, Associate Director from 2017 to 2018, Sr. Manager of Quality Business Analytics from 2015 to 2017, and Manager of Customer Complaints from 2010 to 2015, Paul demonstrated a diverse range of expertise and responsibility within the company.
Early Career and Roles at Merck and GQSCM
Before his tenure at Celgene, Paul Costantini worked at Merck as a Manager for seven years from 2003 to 2010. He also held positions at GQSCM as Supervisor from 2001 to 2003 and Senior Project Coordinator from 2000 to 2001. His early professional experience provided a foundation in management and coordination within the pharmaceutical industry.
Education and Academic Background
Paul Costantini pursued his higher education at Drexel University, obtaining a BS in Mechanical Engineering. His academic tenure lasted from 1986 to 2001. The extensive period of study demonstrates a deep commitment to his field, which he has successfully applied throughout his career in various technical and managerial roles.
Expertise in Quality and Risk Management Systems
With a strong background in user acceptance testing and defect management for GxP systems, Paul Costantini has extensive experience managing electronic document management systems (EDMS) and risk management platforms. He is well-versed in the Veeva and eTQ platforms, highlighting his capability in overseeing deviations, CAPA, and change control systems within the pharmaceutical industry. His track record includes identifying improvement opportunities for products and processes.