Vered Kivity Email
VP Regulatory and Clinical Affairs @ Bonus Biogroup
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Vered Kivity Location
- Israel
Vered Kivity Work
- 2022 -now VP Regulatory and Clinical Affairs @
- 2020 -now Head Of Regulatory and Clinical Affairs @
- 2018 -2020 CMC Manager @
- 2016 -2018 Manager of Regulatory Affairs @
- 2015 -2016 Senior Project Manager, Regulatory Affairs @
- 2012 -2015 Project Manager @
- now Project Manager @
- 2007 -2010 Director of Product Development and Regulatory Affairs, Business Development Manager @
- now Director of Product Development and Regulatory Affairs, Business Development Manager @
Vered Kivity Education
- Technion - Israel Institute of Technology
Post Doc (Biotechnology)
2004-2007 - Technion - Israel Institute of Technology
PhD in Biology
1999-2003 - Technion - Israel Institute of Technology
MBA
2000-2002 - Technion - Israel Institute of Technology
BA (Biology)
1997-1999
Vered Kivity Skills
- Biotechnology
- Tissue Culture
- R&D
- Cell Biology
- Biochemistry
- Molecular Biology
- Cell Culture
- Research
- PCR
- Lifesciences
- Regulatory Affairs
- Regulatory Submissions
- Project Management
- Clinical Trials
- Clinical Research
- Life Sciences
- Diagnostics
- ELISA
- Protein Chemistry
- Pharmaceutical Industry
- FDA
- Product Development
- Research and Development (R&D)
- Business Development
- Medical Devices
- Leadership
- Public Speaking
- Management
- CE marking
- Research and Development R&d
- Research and Development
Vered Kivity Summary
- Vered Kivity, based in Israel, is currently a VP Regulatory and Clinical Affairs at Bonus BioGroup. Vered Kivity brings experience from previous roles at Bonus BioGroup, EQUASHIELD® and Protalix Biotherapiutics. Vered Kivity holds a 2004 - 2007 Post Doc in Biotechnology @ Technion - Israel Institute of Technology. With a robust skill set that includes Biotechnology, Tissue Culture, R&D, Cell Biology, Biochemistry and more. Vered Kivity has 3 emails on RocketReach.
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