Susan Genseberger's Location
Netherlands
Susan Genseberger's Work
- Director Regulatory Affairs @ Gilead Sciences
- Sr Manager Regulatory Affairs @ Gilead Sciences
- Manager Regulatory Affairs @ Gilead Sciences
- Manager Regulatory Affairs and Quality Assurance and Responsible Person @ BGP Products B.V. , Mylan EPD
- Manager Regulatory Affairs and Quality Assurance and Responsible Person @ AbbVie
- Senior Regulatory Affairs Associate @ AbbVie
- Ad-Interim Manager Regulatory Affairs and QA @ AbbVie
- Head of Global Regulatory Affairs Quality Systems @ AbbVie
- Head of Global Regulatory Affairs Quality Systems @ Solvay Pharmaceuticals
- Regulatory Expert @ Solvay Pharmaceuticals
Susan Genseberger's Education
- Universiteit van Amsterdam
Msc (Chemistry)
1989 - 1995 - Pieter Nieuwland College
Atheneum
1985 - 1989 - Bijlmerdrie1974 - 1977
Susan Genseberger's Skills
- Regulatory Affairs
- Pharmaceutical Industry
- Regulatory Submissions
- eCTD
- GMP
- V&V
- CMC
- Validation
- Sop
- Quality System
Susan Genseberger's Summary
Susan Genseberger, based in Netherlands, is currently a Director Regulatory Affairs at Gilead Sciences, bringing experience from previous roles at Gilead Sciences, BGP Products B.V. , Mylan EPD and Abbott B.V.. Susan Genseberger holds a 1989 - 1995 Msc in Chemistry @ Universiteit van Amsterdam. With a robust skill set that includes Regulatory Affairs, Pharmaceutical Industry, Regulatory Submissions, eCTD, GMP and more, Susan Genseberger contributes valuable insights to the industry. Susan Genseberger has 2 emails on RocketReach.
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