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 JOACHIM ERMER
Dr Ermer worked for almost 30 years in various positions in industrial Quality Control. His responsibilities included head of laboratory within the analytical drug development at Hoechst AG, Frankfurt, Germany, a global function as Director of Analytical Processes and Technology at Aventis, head of Quality Control and head of QC Lifecycle Management Frankfurt Chemistry, Sanofi, Germany, and Sanofi Global Reference Standard Coordinator. Since December 2020, he serves as consultant for topics of pharmaceutical analytics and Quality Control.
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 GERALD KINDERMANN
Dr Kindermann was Product Quality Manager at the Global Quality Group at Roche working on quality systems. Before that he was Group Leader Quality Control and Quality Manager for the Supply Center. In May 2023, he joined GxP Consulting, in Basel, Switzerland as a Senior Consultant in the GMP area.
DR ZVONIMIR MAJIC
IATA Senior consultant for Healthcare, Croatia. Former Global Director for supply chain quality assurance and GDP in Teva Pharmaceutical Industries Ltd. Since 2010, he has been an active member of Parenteral Drug Association, SC Interest Group steering committee in Europe, under which he has co-authored several Technical reports on GDP.
DR BOB MCDOWALL
Analytical chemist with over 30 years experience including 15 years working in the pharmaceutical industry with 2 multinational companies.
MARKUS MULTHAUF
Senior Consultant GMP-Engineering Markus Multhauf studied process engineering. He has worked for HOECHST and for plant construction companies like Waldner and Hager+Elsasser. At LSMW/M+W he was design engineer for utility systems and project manager for 9 years. Then he was head engineering at Aeropharm (SANDOZ/ Novartis). Since 2013 he has been a freelancing engineer for pharmaceutical technology.
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.
YVES SAMSON
Yves joined the industry where he served as project and site engineer automation. In 2002, he founded Kereon AG. He is member of GAMP® Europe Steering Committee, co-founder and chairman of GAMP® Francophone and edited the French version of GAMP® 4 / 5. Membership: ECA ‘DI & IT Compliance Group’.
DR HARALD STAHL
Head of Strategy & Business Development - Dr Stahl is a physicist, worked in the Pharmaceutical Development of Schering and was responsible for evaluating new technologies for many years as Group Director Application & Strategy Management at GEA. He is currently Head of Strategy & Business Development at Romaco.
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 INGRID WALTHER
Dr Walther has more than 25 years professional experience in the pharmaceutical industry and in GMP consulting.
ROBERT G. SCHWARZ
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
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
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.