Experience

Cristalens International

• France
• Medical Device
• 1 - 100 Employee

• Pharmacist in charge of Post Market regulatory affairs

  • Oct 2022 - Present

  Lannion, Bretagne, France ➤ Coordinator of the Quality, Clinical and Regulatory teams for the PMS system ➤ Drafting and implementing procedures for the Post Market Surveillance System: MDR 2017/745 ➤ Drafting PMS reports for Intraocular lenses (Class IIb Medical Devices) ➤ Raising awareness of the staff in Post Market Surveillance System ➤ Support for international registrations



Seenel Imaging

• France
• Medical Device
• 1 - 100 Employee

• Quality Assurance and Regulatory Affairs Officer (QARA)

  • Mar 2021 - Sep 2021

  Lille, Hauts-de-France, France ➤ Drafting CE marking file for an electroencephalogram helmet - European Medical Device Regulation 2017/745 ➤ Drafting and implementing the Quality Management System - ISO 13485 ➤ Raising awareness and training of the staff in quality procedures



Hospices Civils de Lyon - HCL

• France
• Hospitals and Health Care
• 700 & Above Employee

• Steril Medical Devices Pharmacy Hospital

  • Jul 2019 - Aug 2020

  ➤ Medical Device Vigilance Reporting ➤ Traceability of dental implants and the VAC®/AbThera® devices (for Negative Pressure Wound Therapy) ➤ PharmD Thesis: "Les biomatériaux pour la régénération osseuse et la gestion des tissus mous en odontologie: état des lieux" ➤ EuroPharmat Poster: "Platelet Rich Plasma: Characteristics of Collection Systems"