Robert Zoubek

Robert E. Zoubek, PhD, joined Granzer Regulatory Consulting & Services in October 2013. Robert supports our clients in all questions concerning drug development, manufacturing and quality control. As expert he is frequently invited to give talks and lead workshops on international conferences.

Robert has more than 10 years of experience in the development of pharmaceuticals. Until he joined Granzer Regulatory Consulting & Services, Robert worked in several positions at Formycon (former Scil Technology) and GlycoForm in the UK.

As Director Scientific Affairs he led Formycon´s drug product development and analytical services. He advised numerous clients on their development strategies, planned and accompanied their projects through the different development stages.

Before that, Robert was Head of Protein Characterisation & Preformulation and Manager Quality Operations. In those positions he supervised Formycon´s Quality Control and was responsible for the GMP compliant organisation of the certified laboratories. He also worked at GlycoForm in Abingdon, UK. As research biologist, he contributed to the development of Biobetters based on GlycoForm´s expertise to chemically synthesize complex glycan structures.

Key knowledge areas:

• CMC
• Pharmaceutical development
• Biosimilar development