Kate Skinner Email & Phone Number | Over 25 years of demonstrated expertise in the pharmaceutical industry, with skills in the areas of technical writing, computer validation documentation and change management processes - with special emphasis on providing project support services and client satisfaction. Specialties: Technical Writing/Computer Validation Documentation, Test Script Creation & Execution, Change Management – Process & Documentation , Process & Procedure Development, Project Coordination, System Migrations & Implementations, Global Team Experience, Validation Plans, IQ/OQ/PQ protocols, SOPs, SWIs, ISPs, 21 CFR Part 11 SKILLS • Pharmaceutical technical writing – based on the GMP validation approach • Hardware: IBM and Apple-compatible desktop and laptop computers • Software: MS Windows, W2000/XP+, MS Office 2000+/XP (including Visio), Documentum-based document management systems, MicroStrategy

Kate Skinner

Over 25 years of demonstrated expertise in the pharmaceutical industry, with skills in the areas of...
North Wales, Pennsylvania, United States

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Kate Skinner’s Location North Wales, Pennsylvania, United States

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Kate Skinner’s Prior Industry Icon Clinical Research | Sanofi Pasteur | Sanofi Aventis Pharmaceuticals

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Technical Writer - Medical Imaging

2015-06-01 00:00:00 - 2018-03-01 00:00:00

IS Business Analyst – Commercial Operations (contractor)

2012-01-01 00:00:00 - 2015-05-01 00:00:00

IS Desktop Solutions Analyst

1986-01-01 00:00:00 - 2001-01-01 00:00:00

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Kate Skinner is a Over 25 years of demonstrated expertise in the pharmaceutical industry, with skills in the areas of technical writing, computer validation documentation and change management processes - with special emphasis on providing project support services and client satisfaction. Specialties: Technical Writing/Computer Validation Documentation, Test Script Creation & Execution, Change Management – Process & Documentation , Process & Procedure Development, Project Coordination, System Migrations & Implementations, Global Team Experience, Validation Plans, IQ/OQ/PQ protocols, SOPs, SWIs, ISPs, 21 CFR Part 11 SKILLS • Pharmaceutical technical writing – based on the GMP validation approach • Hardware: IBM and Apple-compatible desktop and laptop computers • Software: MS Windows, W2000/XP+, MS Office 2000+/XP (including Visio), Documentum-based document management systems, MicroStrategy