CQV Engineer / Pharma / West / SGD 6,300!
Summary
Plans and runs validation tests (IQ, OQ, PQ) for pharma manufacturing gear and clean utilities, ensuring compliance with GMP and FDA rules.
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.