Vacancy Description
Responsibilities:
Execute pharmaceutical CSV validation projects including implementation of new systems, remediation of legacy systems, and re-validation activitiesDevelop and execute validation deliverables including Validation Master Plans, IQ/OQ/PQ protocols, summary reports, and impact assessmentsCoordinate with validation, engineering, IT, and quality teams to ensure successful project executionLead cross-functional teams in development and execution of validation activitiesGenerate and review system impact assessments and critical aspect assessmentsEngage end users for URS/FRS documentation generation and testing requirementsDevelop and execute test scripts while supporting troubleshooting and system configuration activitiesManage multiple CSV projects utilizing project management methodologiesSupport development of validation best practices aligned with current industry standards and guidel...
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