CQV Engineer (Pharma) (SG)
Anter Consulting • singapore, singapore • Posted July 09, 2026
About the Role
Job Description
Key Responsibilities
We are seeking a highly skilled CQV (Commissioning, Qualification, and Validation) Engineer to join our team for a significant pharmaceutical project in Singapore. This role involves ensuring that all systems and equipment are properly commissioned, qualified, and validated in compliance with GMP regulations.
Key Responsibilities
- Oversee the commissioning of pharmaceutical manufacturing equipment and systems to ensure they meet design specifications and regulatory requirements.
- Develop and execute qualification protocols (IQ, OQ, PQ) for equipment, utilities, and systems.
- Ensure that all processes are validated according to industry standards and GMP regulations.
- Prepare and maintain detailed documentation for all commissioning, qualification, and validation activities, including protocols, reports, and traceability matrices.
- Ensure all activities comply with GMP regulations...