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.