CQV EngineerDesign Documentation: URS, FRS, DS, and other engineering specificationsValidation Processes: IQ, OQ, PQ, Process Validation (PV), Computer Systems Validation (CSV), Master Validation Plan (MVP)Quality Systems: Change Control, Non-Conformances, Requalification protocols (IQ/OQ/PQ) in compliance with GMP, FDA, and other regulatory requirementsRegulatory Compliance: Understanding of cGxP principles, ISO 13485, ISO 14971, and 21 CFR 820CQV Leadership: Leading CQV efforts for new and existing systems, troubleshooting issues, collaborating with cross-functional teams, preparing detailed validation documentation, and ensuring regulatory compliance