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Overview Role Overview Responsible for Computer System Validation activities within a pharmaceutical manufacturing environment. Responsible for the development and execution of key validation and quality documentation including Qualification Plans, Test Plans, Requirements Traceability Matrices (RTMs), and Validation
Overview PM Group is looking for a DevOps Lead to join a pharmacetiocal client of ours in Limerick. Responsibilities Design, implement, and maintain CI/CD pipelines to support reliable and repeatable MES deployments across development, test, and production
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