Hanane SIMMOU has a diverse work experience. From March 2014 to March 2021, they worked at Laboratoires Lehning, where they started as an Intern in Regulatory Affairs and progressed to become an International Regulatory Affairs Project Manager. Prior to that, they had an internship at Groupe IMT from December 2013 to February 2014. In 2021, they joined I-VIRTUAL as a Quality Assurance and Regulatory Affairs Engineer and later became the Deputy Head of Quality and Regulatory Affairs in July 2022.
Hanane SIMMOU completed their education as follows:
- From 2013 to 2014, they attended Faculté de Pharmacie de Tours and obtained a Master 2 in Production et Réglementation des Produits de santé, specializing in Pharmacotechnie, Contrôle Analytique, Affaires Technico-Réglementaires.
- In 2012 and 2013, they studied at Faculté de Médecine de Nancy - Université de Lorraine, where they earned a Master 1 in Ingénierie de la Santé et Sciences du Médicament, focusing on BioIngénierie et Médicaments.
- In 2011 and 2012, they pursued a Bachelor's degree in Sciences du Vivant, specializing in Biochimie et biologie moléculaire at Universite de Lorraine.
- In 2010 and 2011, they completed their first year of studies in Sciences du Vivant, again specializing in Biochimie et biologie moléculaire at Universite de Lorraine.
- From 2008 to 2010, they attended Faculté de Pharmacie - Université de Lorraine, where they completed the Premier Cycle des Etudes de Pharmacie (PCEP1).
- Hanane completed their secondary education at Lycée Jean-Victor Poncelet from 2005 to 2008, obtaining a Baccalauréat Scientifique.
Additionally, Hanane SIMMOU has obtained several certifications:
- In April 2023, they received certification in "La gestion des risques pour les dispositifs médicaux selon la norme ISO 14971 v.2019" from AFNOR Certification.
- In November 2022, they obtained the certification "Maîtriser le dossier réglementaire pour obtenir l'homologation FDA" from IFIS - Institut de Formation des Industries de Santé.
- In June 2022, they received certification for "Comprendre la norme ISO 13485 V.2016 et ses exigences" from AFNOR Certification.
- In March 2022, they obtained the certification "Règlement DM (MDR): du marquage CE à la mise sur le marché" from IFIS - Institut de Formation des Industries de Santé.
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