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Carsten Buschmann studied Chemistry in Bielefeld and Marburg. From 1998 to 2006, he worked at A&M Labor GmbH, an analytical service laboratory for the pharmaceutical industry operating under GMP and GLP standards. As the GLP Study Director, he was responsible for conducting and reporting the analytics of preclinical studies. From 2006 to 2018, Carsten Buschmann worked at Grünenthal GmbH, initially as a Quality Assurance (QA) representative in Analytical Chemistry, and later he led the GMP QA department in the Research and Development division. In this role, he conducted audits worldwide on pharmaceutical manufacturing, quality control, and IT, both internally and at service providers. Since 2019, he has been working at Bayer AG in the GMP QA department for Research and Development, focusing on quality assurance in Analytical Equipment Qualification and Computerized Systems. He is also a lecturer on "Quality Assurance" at the Bonn-Rhein-Sieg University and a member of the APV Information Technology focus group.