We are seeking a motivated and detail-oriented Validation / CQV Engineer to support qualification and validation activities in a regulated pharmaceutical/biotech environment. The ideal candidate will have hands-on experience in IQ/OQ execution, Computer System Validation (CSV), and validation documentation while ensuring compliance with regulatory standards including 21 CFR Part 11, ALCOA principles, and GAMP guidelines. The role involves working with laboratory systems and environmental monitoring (EM) systems to support compliance, quality, and operational readiness.

• Execute and document IQ/OQ (Installation Qualification / Operational Qualification) protocols and activities.


• Support Commissioning, Qualification, and Validation (CQV) activities for laboratory and manufacturing systems.


• Perform Computer S...