Computer Validation Specialist - Greenville
1 day ago

Job summary
We are seeking an experienced Validation Analyst / CQV / CSV Engineer to support Steriles Manufacturing operations within a regulated GxP pharmaceutical environment.Responsibilities
- Develop, execute and document Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ) protocols.
- Prepare and maintain Validation Summary Reports (VSRs) summarizing validation activities nd documentation.
Job description
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