Autoren

1989 University degree in Pharmacy

1990-1995 Doctorate in Pharmaceutical Technology
(University of Saarland, Germany)

1995-1997 Fresenius AG (Bad Homburg, Germany), Production of large volume parenterals: Assistant of head of manufacturing, different projects dealing with GMP upgrade and productivity improvement

1998 Fresenius AG (Friedberg, Germany): Production of large volume parenterals:
Head of different manufacturing lines, deputy head of manufacturing for complete production facility according to German Drug Law

1998-2006 Pharmaplan GmbH (Bad Homburg, Germany):
Consulting activity for pharmaceutical industry with regards to qualification, validation, GMP-Compliance
Project manager for many national and international projects

2004 Head of department Qualification, Validation and GMP-Compliance

2007-2008 Fresenius Kabi AG (Bad Homburg, Germany) Corporate Quality Management:
Director QS-Systems and Compliance. Qualified Person third party manufacturing for Fresenius Kabi Germany

since 2008 Fresenius Kabi AG (Bad Homburg, BU Compounding):
Director Technologies and QM Compounding.

Publications at Maas & Peither GMP Publishing:

• GMP-MANUAL
  (Author of chapter 3.F Building services and chapter 3.H Process Gases)