Bordeaux Area, France
IS Compliance & Validation expert at CVOEurope
Pharmaceuticals
Education
Université Bordeaux I, II 1985 — 1989
Maitrise Biochimie + DUT Informatiqe
Experience
PF, Novartis, Ipsen, Hemodia, Arkopharma, PMI, Chiesi 2007 - Present
CVO-Europe April 2005 - Present
Sopra + CVO-Europe October 2001 - Present
CVO - Europe 2005 - 2012
sanofi-aventis October 2001 - March 2010
Ipsen 2010 - 2010
Skills
ERP, Pharmaceuticals, Risk Assessment, Business Continuity, Document Management, Change Management, V&V, SOP, GAMP, Regulatory Submissions, Quality System, Quality Assurance, Pharmaceutical Industry, Change Control, Quality Systems, Regulatory Affairs, Audit, cGMP, Auditing, GMP, Risk Management, CAPA, Computer System..., Compliance, Sop, Quality Management, Manufacturing, Risk Analysis, FDA, Validation, ITIL, LIMS, GxP, Testing, 21 CFR Part 11, Process Validation, Software Validation