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The CSV Engineer will develop and execute validation protocols/documents, manage change controls, participate in audits, troubleshoot issues, assess compliance of systems, and coordinate with departments or contractors to maintain regulatory adherence in computer validation processes.

The Project Manager will lead cGMP initiatives, managing mid-sized to large projects in the Life Sciences sector, focusing on commissioning and validation activities. Responsibilities include oversight of CQV services, document management, progress tracking, and resource allocation to ensure project deliverables are met efficiently.