Professional GMP Trainers

Our trainers have been working for us as speakers over many years. Only GMP trainers who have performed successfully at our open GMP Education courses or European conferences can conduct in-house trainings on our behalf.

The following list contains GMP trainers who are involved in many customised training courses.

DR RAPHAEL BAR
Dr Bar headed the Analytical R&D Laborato ries at Teva Pharmaceuticals and the analytical QC laboratory at Pharmos. Today, he works as trainer and consultant.

DR CHRISTOPHER BURGESS
Chris Burgess is a chemist with more than 30 years experience in the pharmaceutical industry, which he mostly gathered in quality assurance and analytical R&D at Glaxo.

DR MARCEL GOVERDE
Mr Goverde led the QC Labs for non-sterile product testing at F. Hoffmann-La Roche Ltd. and he worked as a QC expert for microbiology at the chemical department of Novartis Pharma.

DR JOSEF M. HOFER
Dr Hofer headed the department International Drug Regulatory Affairs of Klinge Pharma in Munich, Germany.

DR AFSHIN HOSSEINY
Afshin Hosseiny was Director of Quality Assurance for the Global Supply Network of GlaxoSmithKline. He also is a Qualified Person under permanent Provisions.

DR BOB MCDOWALL
Analytical chemist with over 30 years experience including 15 years working in the pharmaceutical industry with 2 multinational companies.

GERT MOELGAARD
Gert Moelgaard has been Vice President for Innovation & Business Development in NNE Pharmaplan.

DR BETTINA PAHLEN
During the last 15 years she has been working at the university, in authority and in different areas of the pharmaceutical industry (R&D, manufacturing, quality control, quality assurance).

DR HEINRICH PRINZ
Heinrich Prinz can look back on many years working for Boehringer Mannheim (Roche Diagnostics), and Biotest AG in both QA and QC.

DR BERND RENGER
Dr Renger was Director of QC at Vetter Pharma-Fertigung. He started his career at Hoechst AG as a research and development chemist. Since then, he held several positions at Mundipharma, Altana Pharma and Baxter. He also is a Qualified Person under the permanent provisions.

DR WOLFGANG SCHUMACHER
Dr Schumacher has more than 30 years experience in the pharmaceutical Industry. At Hoffmann-La Roche he established the IT quality assurance department and was accountable in Technical Operations as Vice Director for the GMP/CSV compliance of all global computer systems and the setup of the Data Integrity program.

DR PAUL STOCKBRIDGE
Dr Stockbridge spent 23 years with Eli Lilly, initially in fermentation development and then in quality assurance. He then moved to Aventis Pharma before being appointed Corporate Quality Director for Cobra Biomanufacturing Plc. He is now providing independent consulting and training services for the steriles, aseptic and biotechnology industries.

DR INGRID WALTHER
Dr Walther has more than 25 years professional experience in the pharmaceutical industry and in GMP consulting.

Dr Hiltrud Horn´s focus is on CMC, GMP and Regulatory Affairs (EU and US). She started in pharma industry in 1990 and held several managerial positions within Hoffmann-La Roche and Knoll (now Abbott) with global responsibility within QC / QA / Regulatory Affairs / Project Management / Medical Writing. She was consultant for the biotech and life science industry at Cap Gemini Ernst & Young prior to starting her own business.

Robert Schwarz joined Shire (formerly Baxter), Vienna in 2001. Until 2005 he was coordinator of environmental monitoring. From 2005 until 2018 he was validation specialist responsible for equipment qualification, sterilization validation and cleaning validation. He is university lecturer in the field of biotech (core topics validation/qualification, aseptic processing, cleanroom technologies and QC).

Prabjeet Dulai was the Responsible Person for GDP and Senior Supply Chain Pharmacist for the UK Ministry of Defence before starting working as a consultant. She also worked as a Pharmacist within the NHS/private hospital sector, retail and pharmaceutical industry.

Dr Ulrich Kissel is Qualified Person and Member of the Board of Directors of the European Qualified Person Association (EQPA). He works as a GMP consultant and contract QP to the Pharmaceutical Industry. Previous to his current role he held leadership positions in Quality and Supply Chain and served for many years as QP for Roche.

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