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Responsibilities Automation Change (IRIS) Review and Approval Review and Approval of Automation Designs Installation and Operation Qualification (IOQ) Protocol Generation Execution and Reporting for DeltaV (PAS) Test specification pre-approval review and post approval prior to progression to IOQ Co-ordination of changes to ensure timely delivery 6+ years Validation experience in a GMP environment.
Strong attention to detail Capacity to organize work and report status to a high standard Ability to work within site Quality procedures Familiarity with DeltaV Bachelors Degree in appropriate field of study or equivalent work experience To be considered for this role you will be redirected to and must complete the application process on our careers page. xcfaprz
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