Marcus Gould Email & Phone Number
Regulatory Affairs Officer @ TestCard.com
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Marcus Gould Location
- United Kingdom
Marcus Gould Work
- 2021 -now Regulatory Affairs Officer @
- 2020 -2021 Director of RA and QA @
- 2020 -2021 Director of RA and QA @
- 2019 -2021 Director of RA and QA @
- 2019 -2021 Head of RA and QA @
- 2019 -2021 QMS Manager @
- 2019 -2021 Head of RA and QA @
- 2017 -2021 RA and QA Consultant @
- 2017 -2021 Head Of Quality Assurance @
- 2019 -2021 Head of RA and QA @ Arthronica
- 2018 -2020 QMS Consultant @
- 2015 -2020 RA and QA Consultant @
- 2019 -2020 Head of RA and QA @
- 2017 -2020 Director of RA and QA @ MW Diagnostics
- 2018 -2019 Head of RA and QA @ Symimetic Ltd
- 2019 -2019 Regulatory Intelligence Consultant @
- 2018 -2018 Senior Regulatory Affairs Consultant (Contract) @
- 2017 -2017 RA and QA Consultant @
- 2017 -2017 RA Consultant @
- 2015 -2017 RA and QA Consultant and Interim Regulatory Affairs Director @
- 2014 -2017 Regulatory Affairs Manager @
- 2016 -2016 RA Consultant @ Healthup | AioCare
- 2015 -2015 RA Consultant @
- 2011 -2014 EMEA Senior Regulatory Affairs Associate, Medical Devices @
- 2009 -2011 Regulatory Affairs and Quality Assurance Manager @
- 2008 -2009 Founder and Managing Director @ Oxford Spires Tutorials
- 2007 -2009 Postdoctoral Research Associate @
Marcus Gould Education
- Regulatory Affairs Professionals Society (RAPS)
Regulatory Affairs Certificate: Medical Devices (Medical Devices)
2010-2010 - University of Oxford
DPhil (Biochemistry - molecular microbiology)
2002-2006 - The University of Birmingham
MPhil (Research) (School of Biosciences Graduate Safety Officer)
2001-2002 - The University of Birmingham
BSc (Hons) (Biology specialising in Microbiology)
1998-2001
Marcus Gould Skills
- Regulatory Affairs
- ISO 13485
- GMP
- FDA
- Regulatory Submissions
- Medical Devices
- Regulatory Requirements
- CAPA
- Biotechnology
- SOP
- Quality System
- Change Control
- R&D
- Design Control
- CE marking
- GLP
- 510(k)
- In Vitro Diagnostics
- Regulatory Strategy Development
- R & D
- Scientific Writing
- U.S. Food and Drug Administration (FDA)
- Research and Development (R&D)
- Good Laboratory Practice (GLP)
- Standard Operating Procedure (SOP)
- Good Laboratory Practice Glp
- 510k
- Corrective and Preventive Action Capa
- Research and Development R&d
- u.s. Food and Drug Administration Fda
- Standard Operating Procedure Sop
- u.s. Food and Drug Administration
- Research and Development
- Corrective and Preventive Action
- Standard Operating Procedure
- Good Laboratory Practice
Marcus Gould Summary
- Marcus Gould, based in United Kingdom, is currently a Regulatory Affairs Officer at TestCard.com. Marcus Gould brings experience from previous roles at Luas Diagnostics, Linear Diagnostics Limited, NuroKor BioElectronics and Echopoint Medical Ltd. Marcus Gould holds a 2010 - 2010 Regulatory Affairs Certificate: Medical Devices in Medical Devices @ Regulatory Affairs Professionals Society (RAPS) . With a robust skill set that includes Regulatory Affairs, ISO 13485, GMP, FDA, Regulatory Submissions and more. Marcus Gould has 7 emails and 4 mobile phone numbers on RocketReach.
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