Robert Saiz Email & Phone Number
Global Head of Diagnostics - Portfolio Strategy for IVDs and Devices and Regulatory Affairs @ BioNTech SE
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Robert Saiz Location
- San Diego, CA, US
Robert Saiz Work
- 2023 -now Global Head of Diagnostics - Portfolio Strategy for IVDs and Devices and Regulatory Affairs @
- 2017 -2022 GRA Device Team Leader - Digital and Diagnostics (Director Regulatory Affairs) @
- 2012 -2021 Consultant - Program Management and Technical and Clinical and Regulatory Affairs @ RTS Consulting Services
- 2011 -2012 Product Development @ Enigma Diagnostics
- 2010 -2011 Masters Student @
- 2010 -2011 Research and Product Development @
- 2008 -2009 Research and Product Development @ Nanogen
- 2007 -2008 Research and Assay Development @ Althea Technologies, Inc.
- 2000 -2008 Analytical Services @ Althea Technologies, Inc.
- 1994 -1999 Research and Development @ Sequana
Robert Saiz Education
- UC San Diego
Regulatory Affairs for the Biomedical Industry Certificate (Regulatory Affairs)
2012-2012 - UC San Diego
Masters of Advanced Studies (MAS) (Clinical Research)
2010-2011 - San Diego State University
Bachelor's of Science Degree (Cell/Cellular and Molecular Biology)
1991-1994 - Regulatory Affairs Profesional Society
Regulatory Affairs Certificate: Medical Devices (Emphasis: Asia, Canada, Europe, and US Regulations)
Robert Saiz Skills
- Product Development
- Process Simulation
- Biotechnology
- Lifesciences
- Molecular Biology
- PCR
- Assay Development
- Biochemistry
- Validation
- GMP
- ELISA
- FDA
- Cell Culture
- Technology Transfer
- qPCR
- Regulatory Affairs
- Laboratory
- Pharmaceutical Industry
- Genomics
- R&D
- Infectious Diseases
- DNA
- Medical Devices
- Genetics
- real-time PCR
- In Vitro
- Hardware Diagnostics
- GLP
- Genotyping
- Biopharmaceuticals
- Life Sciences
- Medical Diagnostics
- Design Control
- Microbiology
- Molecular Diagnostics
- SOP
- Polymerase Chain Reaction Pcr
- Microsoft Office
- Product Launch
- Regulatory
- Good Laboratory Practice Glp
- Customer Service
- Real Time Pcr
- Consulting
- Clinical Research
- Development
- Real Time Polymerase Chain Reaction Qpcr
- u.s. Food and Drug Administration Fda
- Standard Operating Procedure Sop
- Management
- Research and Development R&d
- Data Analysis
- Research
- Good Laboratory Practice
- Polymerase Chain Reaction
- Real Time Polymerase Chain Reaction
- Research and Development
- Standard Operating Procedure
- u.s. Food and Drug Administration
Robert Saiz Summary
- Robert Saiz, based in San Diego, CA, US, is currently a Global Head of Diagnostics - Portfolio Strategy for IVDs and Devices and Regulatory Affairs at BioNTech SE. Robert Saiz brings experience from previous roles at Sanofi Genzyme, RTS Consulting Services, Enigma Diagnostics and UCSD MAS Program - Clinical Research. Robert Saiz holds a 2012 - 2012 Regulatory Affairs for the Biomedical Industry Certificate in Regulatory Affairs @ UC San Diego. With a robust skill set that includes Product Development, Process Simulation, Biotechnology, Lifesciences, Molecular Biology and more. Robert Saiz has 2 emails and 2 mobile phone numbers on RocketReach.
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