Basel Area, Switzerland
Global Head GMP Audit at Novartis
Pharmaceuticals
Education
University of Alberta 1994 — 1995
Post Doctoral Research, Separation of Oligosaccharide Libraries
The Faculty of Engineering at Lund University 1990 — 1992
Post Doctoral Research, Synthetic Chemistry/Peptide Synthesis
Jadavpur University 1984 — 1989
Doctor of Philosophy (Ph.D.), Chemistry
Experience
Novartis 2013 - Present
AstraZeneca 2011 - 2013
AstraZeneca 2006 - 2011
AstraZeneca 2003 - 2006
BioInvent International AB 1996 - 2003
Skills
Quality Assurance, Technology Transfer, Chromatography, Biopharmaceuticals, Regulatory Requirements, 21 CFR Part 11, Document Management, Project Management, Therapeutic Areas, Pharmaceutics, V&V, Biotechnology, Analytical Chemistry, Drug Discovery, Quality Systems, Formulation, CMC Regulatory Affairs, FDA, SOP, Quality System, Sop, GxP, Life Sciences, Cell Culture, Contract Manufacturing, Validation, Lifesciences, GMP, CTMS, Regulatory Submissions, Cleaning Validation, CAPA, Regulatory Affairs, Quality Auditing, Clinical Development, Research Project..., Cross-functional Team..., Drug Development, CRO, Change Control, Quality Control, GLP, Pharmaceutical Industry, Clinical Trials