Ines Cherif Email

Regulatory Affairs Specialist @ Medtech SA

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Ines Cherif Location

Montpellier, FR

Ines Cherif Work

2024 - now Regulatory Affairs Specialist @ Medtech SA
2023 - 2024 Senior Regulatory Affairs and Quality Assurance Engineer @ Sim&Cure
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2021 - 2022 Regulatory Affairs Specialist @ BioSerenity

2020 - 2021 Chargée Affaires Réglementaires Dispositifs Médicaux @ Prodimed
2019 - 2020 Consultante Affaires Réglementaires @ Pierre Fabre Group
2019 - 2019 Stagiaire Affaires Règlementaires Europe @ Septodont
2018 - 2018 Intership in CMC regulatory @ BIOCODEX
2017 - 2017 Internship in Regulatory Affairs at MERCK laboratory (June 2017 ) @ Merck Group
2016 - 2016 Internship in Pharmacovigilance at the Regional Center of Pharmacogivilance (June and July 2016) @ CHU de Montpellier

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Ines Cherif Education

Université de Montpellier
DU Méthodologie en Evaluation Clinique des Dispositifs Médicaux
2020 - 2021
Université de Montréal
Programme d'échange DESS : Diplôme d'Etude Supérieur Spécialisé en Développement du Médicament (Affaires Réglementaires)
2019 - 2019
University of Montpellier
Master 2 Environnement Réglementaire International des Entreprises et Produits de Santé (Faculté de Pharmacie )
2018 - 2019

University of Montpellier
DIU Pharmaco-Economie
2018 - 2019
University of Montpellier
(Ingénierie de la santé)
2015 - 2018

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Ines Cherif Summary

Ines Cherif, based in Montpellier, FR, is currently a Regulatory Affairs Specialist at Zimmer Biomet Robotics (formerly Medtech SA). Ines Cherif brings experience from previous roles at Sim&Cure, BioSerenity, Prodimed and Pierre Fabre Group. Ines Cherif holds a 2020 - 2021 DU Méthodologie en Evaluation Clinique des Dispositifs Médicaux @ Université de Montpellier. Ines Cherif has 1 emails on RocketReach.

Ines Cherif Emails

Found 1 emails

@medtechsurgical.com

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