Referenten

Referenten des Pharma-Kongresses 2020:

• Eva-Maria Baumgartner, Syntacoll
  Validation Manager.
  
• Dr. Matthias Beck, Oncotec
  Manager New Business Development.
• Dr. Peter Bosshard, F. Hoffmann-La Roche
  Quality Manager.
• Sinéad Cowman, Lonza
  Global Business Development and Marketing Manager - Informatics.
• Dirk Denecke, Bayer
  Quality Assurance Specialist.
• Zinaid Dzinovic, Novartis
  Program Manager MES.
• Prof. Dr. Regine Eibl, Zürcher University of Applied Science
  Professor.
• Hesham Elrayes, B. Braun
  Senior Auditor.
• Nikolaus Ferstl, Universitätsklinik Regensburg
  Technischer Leiter.
• Klaus Feuerhelm, Regierungspräsidium Tübingen
  GMP-Inspektor.
• Matthias Freundel, IPA Fraunhofer
  Gruppenleiter Digital Lab Services.
• Holger Frey, Merck KGaA
  Manager of the qualification group within Pharmaceutical Technology.
• Ralf Gengenbach, Gempex
  Managing Director.
• Fabio Gentilini, BSP Pharmaceuticals
  Project Manager.
• Dr. Heidi Gong, Henlius
  Senior Director.
• Hannah Greiner, Fresenius Kabi Austria
  Director Quality Assurance, Innovation & Development Generics & Complex Formulations Graz.
• Dr. Friedrich Haefele, Formerly Boehringer Ingelheim Pharma
  Formerly Head of the department Biopharma Fill & Finish Germany.
• Dr. Martin Haerer, Rommelag CMO
  Head of Development / QP.
• Uwe Harenberg, GESA
  Managing Director.
• Lars Heppert
  Ehemals Director Analytics, CSL Behring.
• Dr. Philip Hörsch, Vetter Pharma-Fertigung
  Director QA - Validation/Risk Management/Trending.
• Dr. Michael Jahnke, Octapharma
  Senior Quality Advisor.
• Oliver Kärst, Merck
  Director Global Packaging Reliability Engineering.
• Alan Kelly, Takeda
  Head of Vaccines - Global Engineering.
• Maria Kladi, National Organization for Medicines, Greece
  GMP Inspector.
• Dr. Johannes Krämer, CSL Behring
  Leiter des Engineerings.
• Dr. Timo Krebsbach, HHAC Labor Dr. Heusler
  Managing Director.
• Günther Kurta, Boehringer Ingelheim
  Head of technical documentation RCV.
• Peter Larsson, Novo Nordisk
  Head of Engineering Management in Novo Nordisk.
• Jens Laucht, CSL Behring
  IT Security Architect for Manufacturing Automation.
• Dr. Markus Lesch, Vetter Pharma-Fertigung
  Head of  Microbiological Validation.
• Prof. Dipl.-Ing. Franz Maier, zuletzt Nycomed
  Zuletzt Leiter der Hauptabteilung Technik.
• Quentin Majeau, Hydro-Fill
  Director of the Single-Use Department.
• Ronan McGarvey, AbbVie
  Director,  Quality Operations.
• Didier Meyer, DMCompliance
  Consultant at DMCompliance.
• Gert Moelgaard, ECA Validation Interest Group
  Chairman; Moelgaard Consulting.
• Dr. Daniel Müller, Local GMP Authority of Baden Württemberg
  Head of GMP Inspectorate.
• Dr. Rainer Nicolai, F. Hoffmann-La Roche
  Projektleiter.
• Dr. Felix Oehme, Bayer
  Head of Biological Development Wuppertal.
• Dermot O'Riordan, EirGen
  Sterile Technical Operations Manager.
• Maarten Pennings, BiosanaPharma
  Chief Technical Officer.
• Dr. Ralf Ratke, AbbVie
  Director Biologics QA.
• Dr. Bernd Renger, Immediate Past Chair of the European QP Association
  Bernd Renger Consulting.
• Dr. Beate Reutter, Landesamt für soziale Dienste Schleswig-Holstein, Kiel, Germany
  GMDP-Inspector and head of the inspectorate.
• Markus Ries, CSL Behring
  Gesamtprojektleiter der Projekte Phoenix und Sphinx.
• Dr. Gabriele Sabine Roidl, Lonza
  Project Leader Drug Product Manufacturing.
• Matthias Runge, Bayer
  Global Manufacturing Systems Technology Expert.
• Yves Samson, ECA DI & IT Compliance Interest Group
  Kereon AG, CEO & e-Compliance SME.
• André Schlierkamp, Bayer
  Head of Quality Data Management.
• Stefan Schöttle, Roche Diagnostics
  Nach 20 Jahren in der zentralen Informatik leitete Herr Schöttle bis zu seinem Vor-Ruhestand
  die Roche Pharma Informatik am Standort Mannheim.
• Dr. Martin Schwab, Vetter Pharma-Fertigung
  Director Customer Project Management.
• Dr. Thomas Schwarz, Novartis
  Leiter Strategische Planung.
• Leslie Southam, Oxford Biomedica
  QA Manager.
• Dr. Susanne Stocker, Roche Diagnostics
  Senior Advisor Innovation, Technology, and MSAT.
• Klaus Storkebaum, Vetter Pharma-Fertigung
  Releasemanager / Projektleiter.
• Dr. Arno Terhechte, Bezirksregierung Münster
  GMP-Inspektor/GMP Inspector.
• Dr. Frank Thielmann, Takeda
  Director Operational Excellence - Europe.
• Markus Turber, Intuity Media Lab
  Geschäftsführung.
• Francois Vandeweyer, Form. Janssen Pharmaceutica
• Rutger Vandiest, Bavarian Nordic
  Senior Director - Global head of sales, CDMO.
• Dr. Ruud van Stigt, Curium
  EU Manufacturing, Supply Chain & MES Manager.
• Dr. Sofia Venceslau, Genibet Biopharmaceuticals
  Project Manager.
• Patrice Wery, GSK Vaccines
  Business Excellence Secondary - Head of Product Stewards.
• Thomas Wibbeling, Miltenyi Biotec
  Manager Computerized Systems Validation.
• Dr. Jakob Weber, BioNTech IMFS
  Projektmanager.
• Udara Yapa, MSD Animal Health Danube Biotech
  Site Validation Lead.
• Jörg Zimmermann, Vetter Pharma-Fertigung
  Vice President Vetter Development Service, External Affairs.