Cqv Engineer / Pharma / West / Sgd 6,300!

My client is looking out for a CQV Engineer that has the following attributes: Key Responsibilities CQV Protocol Execution: Plan, execute, and document CQV activities (IQ, OQ, PQ) for pharmaceutical manufacturing facilities, utilities, and process equipment. Compliance & Standards: Ensure all documentation and activities strictly adhere to GMP, GAMP 5, ISPE Baseline Guides, and FDA/EMA/PIC/S guidelines. Testing & Troubleshooting: Support FAT, SAT, risk assessments, and technical troubleshooting during equipment setup and operational readiness stages. Cross-Functional Collaboration: Partner with engineering, project, and quality teams to drive execution and resolve validation issues on time. Requirements Degree in Engineering, Life Sciences, or a related discipline. 2–5 years of CQV experience within the pharmaceutical or biotech manufacturing sector. Practical knowledge of cGMP, GAMP 5, and validation lifecycle protocols. Hands-on experience validating clean utilities (WFI, clean steam, HVAC), cleanrooms, or process equipment. How to Apply Interested applicants are invited to submit an updated résumé (in MS Word format) highlighting your relevant experience and project achievements. Contact Person: Tan Jun Jie EA Personnel Reg. No.: R1878852 EA License No.: 17C8502 We regret that only shortlisted candidates will be notified.