Siegfried Schmitt, Principal Consultant, joined PAREXEL Consulting in 2007. He provides consulting services to the medical device and pharmaceutical industry on all aspects of regulatory compliance, particularly the design and implementation of Quality Management Systems and Competitive Compliance. He is the PAREXEL practice lead for Quality by Design. Dr Schmitt’s areas of expertise include all aspects of quality and compliance for systems, processes, facilities and operations for drug substances and drug products, for all types of formulations. He is a seasoned and experienced auditor, providing support to clients pre and post inspections or audits. He has previously held positions in industry as Senior Production Chemist with Roche and global Quality Director with GE Healthcare and as Validation Manager with Raytheon and Senior Lead Consultant with ABB. Dr Schmitt is an active member of various industry associations, including DIA, PDA, RAPS and ISPE, conference presenter and organiser of international events. He is also an accomplished author and editor, and member or chairman of several boards of editors. Dr Schmitt is a Chemist by background and holds Chartered Chemist and Chartered Scientist status. He is a Fellow of the Royal Society of Chemistry.BACK TO SPEAKERS PAGE
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