Experience

Curae Lab

• France
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Quality and Regulatory Affair Manager - Pole nutri - CURAE LAB

  • May 2023 - Present

  In charge of laboratories JALDES, DIETETIQUE ET SANTE and SYNERGIA In charge of laboratories JALDES, DIETETIQUE ET SANTE and SYNERGIA



Laboratoire Jaldes

• France
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Regulatory Affairs & Quality Manager

  • Jan 2015 - Aug 2023

  - Regulatory affairs reponsability for the Cosmetic and food supplement - Management of the assurance quality activities - Food supplements and cosmetic developments - Implementation of the quality management system - Quality functions : Quality assurance, SMQ management, Audits (manufacturing sites / Raw materials suppliers) - Regulatory affairs reponsability for the Cosmetic and food supplement - Management of the assurance quality activities - Food supplements and cosmetic developments - Implementation of the quality management system - Quality functions : Quality assurance, SMQ management, Audits (manufacturing sites / Raw materials suppliers)



Laboratoire Gifrer

• Décines - France

• Regulatory Affairs Manager

  • Sep 2014 - Jan 2015

  - Management, coordination of department activities - Preparation / support of inspections (ANSM / DREAL (Reach) / G Med ) - Control of the advertising and promotional documents - Price dossier management - Management, coordination of department activities - Preparation / support of inspections (ANSM / DREAL (Reach) / G Med ) - Control of the advertising and promotional documents - Price dossier management



Baush & Lomb

• Montpellier Area, France

• Senior Regulatory Affairs Manager Emerging Market

  • Jun 1999 - 2011

  - Management, coordination of department activities - Preparation / coordination & submission of the new products (medicinal product / medical device/ food supplement) - strategic regulatory support on Life Cycle Management - Supervision of the material packaging activities - Control of the advertising and promotional documents - Provide regulatory guidance to multidisciplinary teams to ensure that regulatory activities in Emerging markets are performed in the context of approved business activities in time and in compliance with applicable regulatory demands. Show less



Pierre Fabre Group

• France
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Regulatory Affairs Manager

  • Sep 1996 - Jun 1999

  - In charge of the affiliates in Europe (Switzerland/ Spain/ Portugal) and Asia areas. - Review of expert reports / updating of pharmaceutical dossiers - Follow-up of products under license or in development - In charge of the affiliates in Europe (Switzerland/ Spain/ Portugal) and Asia areas. - Review of expert reports / updating of pharmaceutical dossiers - Follow-up of products under license or in development