Jolanda De Bruijne | Senior Director, Head of PV Compliance
Teva Pharmaceuticals

Jolanda de Bruijne, Global Head of Pharmacovigilance Compliance, Teva Pharmaceuticals. In Teva I am responsible for the Pharmacovigilance Compliance strategy and oversight for all Patient Safety aspects across Teva including Pharmacovigilance agreements. The majority of my career I worked on implementing and improving Quality Management Systems across the different GXP regulations (GLP, GMP, GCP, GVP). Before moving the focus to Pharmacovigilance I worked in various global Compliance and Quality roles in the (bio)Pharmaceutical Industry ranging from QP, head of quality control laboratory, auditor and R&D project manager. The last 15 years the focus professionally has been on leading multidisciplinary teams that work on implementing and optimizing Pharmacovigilance Quality Management systems globally, including but not limited to SOPs, Training, EU and local PSMFs, PV Agreements, managing local and global pharmacovigilance inspections and audits, metrics and Data Governance. My areas of interest are Data governance, Artificial Intelligence/ automation and Operational Excellence/ Efficiency.