Mireille Collombat has extensive work experience in regulatory affairs within the pharmaceutical industry. Mireille is currently serving as the VP Head EUCAN Regulatory Affairs at Idorsia Pharmaceuticals Ltd. Prior to this, they held positions such as Senior Director Regulatory Affairs Europe at Luzsana Biotechnology and Jiangsu Hengrui Pharmaceuticals Co., Ltd. Mireille also worked as the EMEA Regulatory Affairs Lead for Pulmonary Hypertension at The Janssen Pharmaceutical Companies of Johnson & Johnson. Mireille spent a substantial part of their career at Actelion, where they held roles including Senior Director, Group Leader, Global Drug Regulatory Affairs, and Director Regulatory Affairs Global Project Leader. Mireille has also worked at Novartis as an Expert Global Regulatory Affairs Manager and Regulatory Affairs Manager. Mireille started their career as a hospital pharmacy resident at AP-HP, Assistance Publique - Hôpitaux de Paris.
Mireille Collombat holds a Pharmacy degree in Pharmaceutical Sciences from the University Montpellier. Mireille also has a Doctor of Pharmacy - PharmD in Pharmaceutical Sciences from the University of Paris V.
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