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Christoph Engelbrecht

Christoph Engelbrecht is a Senior Biotech Consultant with 14 years international CDMO and Biotech work experience. He obtained his training and Master of Science in Biotechnology in Germany, US and Australia.

As an independent consultant Christoph Engelbrecht has successfully completed more than 10 projects since 2015. He helped several European Biotech companies to select the right CDMO, negotiate effective contracts and initiate CMC development up to clinical phase 1 studies.

In his last project Christoph has been responsible for selecting the CDMO, developing & manufacturing an antibody drug product for clinical phase I including filling, labelling, packaging and clinical supply. He managed and supported the preparation of CMC regulatory filing sections (IMPD, CTA) including responses from and to regulatory authorities in Europe and Qualified Person. Furthermore, Christoph has managed the setup of a Quality Management System for this emerging biotech company.

Over the last 14 years Christoph has gained in-depth knowledge and an extensive network in Biotech & CDMO industry. He has direct contact to Biotech Executives and to Business Development Managers and Executives in the Top 20 CDMOs in Europe and Asia.

In a nut shell Christoph Engelbrecht´s strengths and specialties are:

  • CDMO industry knowledge and network in Biologics
  • Negotiating fair services and quality agreements
  • CMC project management
  • Alliance management and business development
  • Collaborations with experienced GxP, regulatory and QA consultants
If you want to accelerate and professionalize your CDMO selection process or need CMC project management and business development support, please do not hesitate to contact us.