Cheryl Ford Email & Phone Number
Contract Project Manager and Technical Writer @ Dicerna Pharmaceuticals, Inc.
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Cheryl Ford Location
- Boulder, CO, US
Cheryl Ford Work
- 2024 -now Contract Project Manager and Technical Writer @
- 1998 -now Owner @ Ford Documentation Service, LLC, now Ford GMP Services, LLC
- 2021 -2024 QC Investigator and NCR Investigator at Agilent NASD @
- 2020 -2021 Contract Technical Writer @
- 2020 -2020 Validation Contractor @ AveXis
- 2020 -2020 Contract Technical Writer @
- 2018 -2019 Contract Technical Writer @ Agilent Nucleic Acids Solutions Division
- 2017 -2018 Contract Compliance Specialist @ Agilent Technologies NASD
- 2016 -2017 Contract Working Project Manager through ValSource @ AstraZeneca
- 2016 -2016 Operations Compliance Specialist @
- 2015 -2016 Senior QA Representative @
- 2011 -2015 Contract Technical Writer @
- 2009 -2014 Contract Technical Writer @ Hospira Boulder
- 2014 -2014 Contract Computer Validation Auditor @ Parexel
- 2014 -2014 Contract Technical Writer @
- 2002 -2004 Contract Project Manager @
- 2000 -2001 Contract Technical Writer and Validation @ NaPro
- 2000 -2001 Contract Technical Writer @ Array BioPharma
- 1994 -1998 Technical Writer @ Roche Pharmaceuticals
- 1994 -1998 Technical Writer @ Roche Colorado (formerly Syntex)
- 1992 -1994 Calibration @ Synergen
Cheryl Ford Education
- University of New Hampshire
Bachelor of Arts (BA) (English Language and Literature, General)
1986-1990 - University of New Hampshire
BA
Cheryl Ford Skills
- Technical Writing
- Validation
- Pharmaceutical Industry
- GMP
- Quality System
- Change Control
- FDA
- Project Management
- Manufacturing
- Sop
- Biotechnology
- 21 CFR Part 11
- Computer System Validation
- CAPA
- Cross-functional Team Leadership
- Process Simulation
- Standard Operating Procedure (SOP)
- U.S. Title 21 CFR Part 11 Regulation
- U.S. Food and Drug Administration (FDA)
- Data Validation
- Compliance
- Operations
- Cross Functional Team Leadership
- u.s. Food and Drug Administration Fda
- Standard Operating Procedure Sop
- Quality Systems
- Standard Operating Procedure
- u.s. Food and Drug Administration
Cheryl Ford Summary
- Cheryl Ford, based in Boulder, CO, US, is currently a Contract Project Manager and Technical Writer at Dicerna Pharmaceuticals, Inc.. Cheryl Ford brings experience from previous roles at Ford Documentation Service, LLC, now Ford GMP Services, LLC, Agilent Technologies, Leiters and AveXis. Cheryl Ford holds a 1986 - 1990 Bachelor of Arts (BA) in English Language and Literature, General @ University of New Hampshire. With a robust skill set that includes Technical Writing, Validation, Pharmaceutical Industry, GMP, Quality System and more. Cheryl Ford has 1 emails on RocketReach.
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