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Sabine Glibert has a strong background in quality management and compliance. Sabine is currently serving as the Vice President of Quality at iSTAR Medical since February 2023. Prior to that, they worked at Cerba Research as the Chief Quality Officer from June 2022 to February 2023 and as the Global Head of QA from May 2021 to June 2022.

Before their role at Cerba Research, Sabine worked at argenx as the Global QA Head of Quality Management System and Training from October 2020 to May 2021. During this time, they focused on building a global team to manage procedural documents and training activities, as well as implementing a new eDMS system and improving employee training quality.

Sabine'sexperience also includes a role as the VP Global Quality Assurance & Compliance at GENFIT from July 2016 to October 2020. In this position, they led the quality assurance and compliance strategies for all R&D and pre-marketing activities, developed and implemented the QMS, and led various programs including vendor qualification, quality metrics, and inspection readiness.

Prior to that, Sabine worked at Bristol Myers Squibb as the Global Vendor Quality Lead & EU Quality Management Associate Director from June 2013 to May 2016, and at ICON plc as the Director Quality Compliance Global Clinical Operations from July 2011 to June 2013. At ICON plc, they developed the global quality compliance department, oversaw site quality assessment visits, and implemented quality metrics and risk-based quality management processes.

Earlier in their career, Sabine served as the Operations Director and Quality Advisor at Aepodia SA from February 2007 to June 2011, where they contributed to company strategy, built a new quality management system, and conducted vendor assessments and audits. Sabine also worked at Eli Lilly & Company as an Operations Team Leader from February 1998 to January 2007, and held positions as a Project Manager at Université catholique de Louvain from August 1996 to January 1998, and as a Researcher at the University of Liège from September 1995 to April 1996.

Sabine Glibert has extensive experience in quality management and compliance, with a focus on developing and implementing effective quality systems and processes in various pharmaceutical and clinical research organizations.

Sabine Glibert holds a diverse educational background. Sabine obtained their first degree, a qualification as a secondary school science teacher, from the Université catholique de Louvain. The specific start and end years for this qualification are not provided. Following this, from 1987 to 1994, Sabine pursued their engineering studies at the same institution, specializing in bio-sciences.

Prior to their higher education, Sabine attended collège Notre-Dame Basse Wavre from 1981 to 1987, where they obtained a degree in humanités. Unfortunately, the field of study for this degree is not specified.

Additionally, Sabine Glibert has obtained a certification as a Data Protection Officer from the Data Protection Institute in July 2021.