CSV Engineer / CQV Engineer - 5W7VRWWR

CQV Engineer – Singapore 

• Responsible for Commissioning, Qualification & Validation (CQV) of pharma manufacturing systems and utilities.
• Execute IQ/OQ/PQ protocols, ensuring compliance with GMP and regulatory standards.
• Coordinate with EPC teams, vendors, and site stakeholders during project execution.
• Support facility start-up, equipment validation, and documentation.
• Drive reliability, safety, and compliance across greenfield and brownfield projects.

CSV / Lab CSV Engineer – Singapore

• Lead Computer System Validation (CSV) activities for pharma and lab IT systems.
• Develop and execute validation plans, risk assessments, and test scripts.
• Ensure compliance with GxP, 21 CFR Part 11, and data integrity standards.
• Collaborate with QA, IT, and engineering teams for system implementation.
• Support Lab CSV projects including equipment qualification, software validation, and audit readiness.