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Eberhard Kwiatkowski worked at Bayer AG after completing his training as a biology laboratory assistant. Initially, he spent three years in the analytical laboratory of biochemical process development. He then managed the biological monitoring laboratory of the medical department at Bayer AG, and later, the residue analysis laboratory for veterinary medicines. Since 1996, he has been involved in the qualification and validation of computerized systems in quality control for active ingredient production. Since 2000, he has been responsible for the validation of computerized systems throughout the Bayer Schering Pharma AG plant in Wuppertal as part of the GMP department for active ingredient production. Mr. Kwiatkowski is a co-author of the ISPE Good Practice Guide for auditing external suppliers and a member of the GAMP DACH Forum.