methodologies, and regulatory compliance. Requirements: IT CSV - Validation of IT systems. CQV - Qualification of Equipment... in authoring validation documents and managing validation projects. Lead and oversee multiple quality and validation projects....
of US FDA (21 CFR 210, 211, 810), ISO 9001, and EU EMEA regulations Knowledge of primary industry guidance on CQV and CSV... is looking for an energetic, self-motivated individual for the role of Director, Operational Readiness. The Director will lead cross-functional...