Jakob Bonde Email
Head of Regulatory Affairs Small Molecules (DS and DP) and Regulatory Affairs Director, CMC @ Lonza
Jakob Bonde's Location
Visp, VS, CH
Jakob Bonde's Work
- Head of Regulatory Affairs Small Molecules (DS and DP) and Regulatory Affairs Director, CMC @ Lonza
- Regulatory Affairs Director, Clinical Trial Regulatory Management and Global Study Start-Up @ Clinipace Worldwide
- Sr. Manager Regulatory and Strategic Development (EU CTA) @ Clinipace Worldwide
- Regulatory Affairs Manager @ Medpace
- CMC Regulatory Affairs and QA Manager @ MondoBIOTECH AG
- CMC and Quality Regulatory Affairs Manager @ Grünenthal Corporate Hub
- Regulatory Affairs Manager Denmark and Iceland and Quality Compliance Officer; Qualified Person @ Johnson & Johnson
- Regulatory Affairs Officer; Delegate QP @ Pfizer
- Trainee, Nervous System Research @ Novartis
- Intern (University Hospital Pharmacy) @ Aarhus Universitetshospital
Jakob Bonde's Education
- Københavns Universitet - University of Copenhagen
Master of Science - MS (Pharmacy)
1996 - 2003 - DTU - Technical University of Denmark
Chemical Engineering
1995 - 1996
Jakob Bonde's Skills
- Regulatory Submissions
- Clinical Trials
- HPLC
- Medical Devices
- Good communication skills
- Flexibility
- Online Communications
- Capability to Adjust in a Changing Environment
Jakob Bonde's Summary
Jakob Bonde, based in Visp, VS, CH, is currently a Head of Regulatory Affairs Small Molecules (DS and DP) and Regulatory Affairs Director, CMC at Lonza, bringing experience from previous roles at Clinipace Worldwide, Medpace Germany GmbH (Prev. Medpace Medical Consulting GmbH) and MondoBIOTECH AG. Jakob Bonde holds a 1996 - 2003 Master of Science - MS in Pharmacy @ Københavns Universitet - University of Copenhagen. With a robust skill set that includes Regulatory Submissions, Clinical Trials, HPLC, Medical Devices, Good communication skills and more, Jakob Bonde contributes valuable insights to the industry. Jakob Bonde has 2 emails on RocketReach.
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