Fiona Day Location
- Bellevue, WA, US
Fiona Day Work
- 2026 -now Director GLP and GCP Quality Assurance @ Zymeworks
- 2024 -2026 Associate Director GLP QA @
- 2024 -2024 Oncology 3rd Party Quality Lead @
- 2021 -2024 Senior Manager GLP Compliance @
- 2020 -2021 Senior Consultant @
- 2019 -2021 Consultant @ ADAMAS Consulting LLC
- 2015 -2019 Senior QA Specialist @
- 2010 -2015 Quality Assurance Auditor- Analytical @
- 2009 -2010 Analytical Study Director @
- 2001 -2004 Associate Director of Inflammation Research @
- 1996 -2001 Senior Scientist @ Corixa Corporation
- 1994 -1996 Postdoctoral Research Fellow @
- 1992 -1994 Postdoctoral Scientist @ Dartmouth Medical School
- 1988 -1992 Graduate Student @ Glasgow University
Fiona Day Education
- The University of Glasgow
PhD, Biochemistry (Biochemistry)
1988-1992 - University of Strathclyde
Bachelor of Science (1st Class Honors), Biochemistry (Biochemistry)
1984-1988
Fiona Day Skills
- Drug Development
- GLP
- Quality Auditing
- CRO
- SOP
- Quality Assurance
- Biotechnology
- Life Sciences
- Audit
- Immunology
- Lifesciences
- FDA
- Immunoassays
- ELISA
- In Vitro
- In Vivo
- Flow Cytometry
- Animal Models
- Biopharmaceuticals
- Clinical Development
- Toxicology
- Good Laboratory Practice (GLP)
- U.S. Food and Drug Administration (FDA)
- Standard Operating Procedure (SOP)
- Good Laboratory Practice Glp
- u.s. Food and Drug Administration Fda
- Standard Operating Procedure Sop
- Auditor
- Good Laboratory Practice
- Standard Operating Procedure
- u.s. Food and Drug Administration
Fiona Day Summary
- Fiona Day, based in Bellevue, WA, US, is currently a Director GLP and GCP Quality Assurance at Zymeworks. Fiona Day brings experience from previous roles at Zymeworks Inc., Pfizer, Seagen and ADAMAS Consulting. Fiona Day holds a 1988 - 1992 PhD, Biochemistry in Biochemistry @ The University of Glasgow. With a robust skill set that includes Drug Development, GLP, Quality Auditing, CRO, SOP and more. Fiona Day has 1 emails and 2 mobile phone numbers on RocketReach.
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