About this role
Job Description Contribute to Life Science projects for Antaes Asia clients. Develop and execute C&Q documentation including commissioning protocols, SAT reports, IQ/OQ/PQ protocols, summary reports, and traceability matrices. Support end-to-end C&Q lifecycle for process, utility, and support systems — e.g. bioreactors, chromatography skids, filtration units, CIP/SIP, WFI, HVAC, autoclaves, and clean utilities. 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 SAT with suppliers and engineering teams. Troubleshoot and resolve technical issues encountered during C&Q execution. Ensure all C&Q 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 coordinate and liase with English speaking counterparts.
What they're looking for
Pharmaceutical IndustryChromatographyGMPHVAC
About Antaes Asia Pte. Ltd.
Industry: Information & communications
Frequently asked questions
What does a Project Engineer at Antaes Asia Pte. Ltd. do?
Job Description Contribute to Life Science projects for Antaes Asia clients. Develop and execute C&Q documentation including commissioning protocols, SAT reports, IQ/OQ/PQ protocols, summary reports, and traceability matrices. Support end-to-end C&Q lifecycle for process, utility, and support system…
What skills does this Project Engineer role need?
Key skills for this role include Pharmaceutical Industry, Chromatography, GMP, HVAC.
How much does a Project Engineer at Antaes Asia Pte. Ltd. pay?
This role lists a salary of S$4,000 – S$7,000 per month.
Is this Project Engineer role remote, hybrid, or on-site?
The listing is based in D01 Marina, Raffles Place, People's Park, Cecil. Check the posting for remote or hybrid options.
How do I apply for this Project Engineer role?
You can apply directly on Antaes Asia Pte. Ltd.'s careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.
