Narcisse BARBOZA

Narcisse Barboza has a diverse range of work experience in quality assurance and regulatory affairs in the medical device industry. Narcisse started their career at NEOLIX, where they worked as a Chargé Qualité/Affaires Réglementaires from March 2011 to June 2012. Narcisse then moved to ab medica sas, where they served as a Coordinateur Qualité/Affaires Réglementaires from December 2013 to June 2015. After that, Narcisse joined Air Liquide as a Chargé Affaires Réglementaires des Dispositifs Médicaux, where they applied European regulations for medical devices, including the EU directive 93/42/CEE. Narcisse worked at Air Liquide from September 2016 to September 2017. Following that, they worked at Aston - SEM (Groupe Acropole) as a Spécialiste Système Qualité des Dispositifs Médicaux from April 2018 to July 2022. In this role, they specialized in ISO 13485, CAPA management, internal and external audits, and risk analysis according to ISO 14971. Currently, Narcisse is the Senior QA/RA Specialist at CAIRDAC, where they support establishment and improvement of the Quality Management System (QMS) and ensures compliance with ISO 13485. Narcisse also contributes to the establishment and maintenance of the Medical Device File and promotes quality policy and culture within the company.

Narcisse Barboza's education history is as follows:

From 2004 to 2008, Narcisse attended Paris-Sud University (Paris XI) and earned a Bachelor's degree in Sciences with a specialization in "Technologies de santé mention chimie" from the Faculty of Sciences in Orsay.

In 2009, Narcisse pursued further education at Paris-Sud University (Paris XI) and obtained a Master's degree in Formulation des médicaments et autres produits de santé at Chatenay-Malabry.

Narcisse continued their education at Paris-Sud University (Paris XI) from 2010 to 2011, completing a Master 2 (M2) program in Contrôle qualité des médicaments de synthèse d'origine naturelle with a specialization in "Dispositifs médicaux" at Chatenay-Malabry.