CQV Engineer
CQV Engineer
Location
D01 Cecil, Marina, People’s Park, Raffles Place
Job Type
Full-time
Experience
Mid
Category
General
Salary
$4,000 - $8,000
Posted
2 days ago
Expires
Feb 11, 2026
Views
1
Job Details
Vacancies
1 position
Experience Required
No experience required
Job Description
Job Description
- Contribute to Life Science projects for Antaes Asia clients
- Develop and execute CQV documentation including commissioning protocols, FAT/SAT reports, IQ/OQ/PQ protocols, summary reports, and traceability matrices.
- Support end-to-end CQV lifecycle for process, utility, and support systems — e.g. bioreactors, chromatography skids, filtration units, CIP/SIP, WFI, HVAC, autoclaves, and clean utilities.
- Participate in design reviews (URS, FDS, P&ID walkdowns) to ensure CQV considerations are integrated during project design and construction.
- Manage execution of commissioning and qualification activities in alignment with project schedules, safety standards, and GMP compliance.
- Support automation qualification (DeltaV, PLC, SCADA) and ensure integration with process control systems.
- Review vendor documentation and coordinate FAT and SAT with suppliers and engineering teams.
- Troubleshoot and resolve technical issues encountered during CQV execution.
- Ensure all CQV deliverables meet internal Quality and Validation standards and align with site Validation Master Plan (VMP).
- Support handover of qualified systems to Manufacturing and Maintenance teams, including training and documentation.
- Collaborate closely with cross-functional teams including Engineering, QA Validation, Manufacturing, and Automation.
- Contribute to the promotion of Antaes services on top of assistance provided to clients
Job Requirements
- Bachelor’s Degree in Chemical, Mechanical, Biomedical, or related Engineering field.
- 3–7 years of CQV experience in the pharmaceutical industry
- Strong understanding of GMP, GEP, ISPE Baseline Guides, ASTM E2500, and FDA/EMA validation expectations.
- Experience in process equipment qualification (bioreactors, chromatography, UF/DF, CIP/SIP), clean utilities, and automation integration.
- Familiar with risk-based CQV approach and change control processes.
- Proficiency with documentation management systems (e.g., Veeva)
- Candidate must be highly motivated, be able to work independently as well as in a team and have good organizational and oral and written communication skills
- Excellent communication skills, both written and verbal, in English - to communicate and work with English speaking counterparts
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ANTAES ASIA PTE. LTD.
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