Validation Specialist
- Employer
- Perkin Elmer
- Location
- Lexington MA US Thousand Oaks CA US Los Angeles CA US
- Closing date
- Jan 25, 2018
View more
- Sector
- Pharmaceutical
- Hours
- Full Time
- Organization Type
- Corporate
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- Design, Author, and Execute Computerized System Validation (CSV) - according to GAMP 5 guidance - especially on Analytical Laboratory Test Equipment and other Lab Information Systems
- Technical Writing of Validtion Documents (Risk Assessment, Validation Plan, Design Configuration/Specification, User Requirements, Functional Requirements, IQ OQ PQ, Trace Matrix, Validation Summary Report), SOPs, Maintenance Procedures, Calibration Procedures, and other instrument support documents
- Translate technical information and requirements into qualification/validation test design
- Contribute to the overall growth of PerkinElmer's compliance business
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