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Franck Diafouka

Head Of Audit (ad Interim) at European Medicines Agency

Franck Diafouka has a diverse work experience spanning various industries. Franck'smost recent position was as the Head of Audit (ad interim) at the European Medicines Agency (EMA), where they conducted operational audits and consulting engagements. Prior to this, they held roles as a Senior Lead Auditor, Head of Division support, Programme Manager, and Head of Department Support at EMA, where they had responsibilities such as coordinating quality systems, business continuity activities, and planning and reporting cycles. Franck also served as a Member of EMA's Audit Advisory Committee. Additionally, they have experience as a Scientific Administrator at EMA's Pharmacovigilance Department. Outside of EMA, Franck has worked as a Senior University Lecturer at the University of Montpellier, a Pharmacist and Dispensary Manager at Boots The Chemists, a Quality Control Manager/Team Leader at Bristol-Myers Squibb, a Pharmacist in Pharmacovigilance and Medical Information (Interim) at Lundbeck, and a Quality Assurance Manager (Interim) at Laboratoires Opodex Industrie. Franck began their career as a Research Associate at CHU Montpellier and as an Associate Research Fellow at CHU de Nimes.

Franck Diafouka earned a Doctor of Pharmacy degree from Faculte de Pharmacie (Universite Montpellier I) between the years 1994 and 2002. Additionally, they pursued a Master CEI in Business, Entrepreneurship, and Innovation from IAE FRANCE - Écoles Universitaires de Management from 2001 to 2002.

Links

Previous companies

Bristol-Myers Squibb logo

Timeline

  • Head Of Audit (ad Interim)

    September, 2022 - present

  • Senior Lead Auditor (internal Audit)

    September, 2015

  • Head Of Division Support (inspections And Human Medicines Pharmacovigilance)

    August, 2013

  • Head Of Department Support (pharmacovigilance & Risk Management Department)

    July, 2010

  • Member Of Ema's Audit Advisory Committee

    October, 2009

  • Programme Manager - Implementation Of EU Pharmacovigilance Legislation

    September, 2009

  • Scientific Administrator (pharmacovigilance Department)

    May, 2006

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