Siegfried Schmitt

Siegfried joined Parexel Consulting in 2007, He provides consulting services to the healthcare industry on all aspects of regulatory compliance, particularly the design and implementation of Quality Management Systems. The services cover the entire product lifecycle, from the clinical to the commercial phase, for all aspects of the Good Practices.

Work Experience

Siegfried’s areas of expertise include all aspects of quality and compliance for systems, processes, facilities and operations for drug substances and drug products. Specifically, he consults on compliant quality systems that integrate industry best practices with future-looking compliance approaches. He has previously held positions in industry as Senior Production Chemist with Roche, Global Quality Director with GE Healthcare, Validation Manager with Raytheon and Senior Lead Consultant with ASEA Brown Boveri Group (ABB).

He is an active member of various industry associations, including DIA, PDA, RAPS and ISPE, conference presenter, and organizer of international events. He is also an accomplished author and editor.

Education

Siegfried is a chemist by background, a Fellow of Royal Society of Chemistry and he holds Chartered Chemist and Chartered Scientist status.