Philippe Vanwolleghem
About Philippe Vanwolleghem
Philippe Vanwolleghem is a Site Manager and Qualified Person with a Master's degree in Pharmacy from Université Catholique De Louvain. He has extensive experience in the pharmaceutical industry, having held various management roles at companies such as Catalent Pharma Solutions, Eli Lilly and Company, and Nycomed Pharma.
Work at IBA
Philippe Vanwolleghem has been employed at IBA since 2008, serving as Site Manager and Qualified Person. In this role, he oversees site operations and ensures compliance with regulatory standards. His tenure at IBA has spanned 16 years, during which he has contributed to various projects and initiatives within the organization.
Education and Expertise
Philippe Vanwolleghem studied at Université Catholique De Louvain, where he earned a Master's degree in Pharmacy from 1987 to 1992. His educational background provides him with a solid foundation in pharmaceutical sciences, which supports his professional roles in the industry.
Background in Pharmaceutical Operations
Prior to his current position, Philippe Vanwolleghem held several significant roles in the pharmaceutical sector. He worked at Catalent Pharma Solutions as Packaging Manager from 2006 to 2008 in Somerset, New Jersey. Before that, he served as Clinical Trial Operations Representative for Europe and Asia at Eli Lilly and Company from 2001 to 2004 in Indianapolis, Indiana. Additionally, he was Head of Production and Deputy Qualified Person at Nycomed Pharma from 1997 to 2001 in Denmark.
Professional Experience at Catalent and Eli Lilly
Philippe Vanwolleghem's professional journey includes notable positions at Catalent Pharma Solutions and Eli Lilly and Company. At Catalent, he worked as Packaging Manager for two years, focusing on packaging operations. His role at Eli Lilly involved clinical trial operations, where he contributed to projects across Europe and Asia for three years.
Leadership Role at Nycomed Pharma
At Nycomed Pharma, Philippe Vanwolleghem served as Head of Production and Deputy Qualified Person from 1997 to 2001. This role involved overseeing production processes and ensuring compliance with quality standards, contributing to the overall efficiency and effectiveness of the operations in Denmark.