Senior CQV Engineer – GMP Validation & Commissioning
Antaes Asia
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Job summary
Antaes Asia in Singapore seeks a CQV validation engineer with 3+ years in the pharmaceutical industry. You will develop and review commissioning protocols, IQ/OQ/PQ, FAT/SAT, and traceability matrices, ensuring compliance with GMP and CSV requirements.
You will support end-to-end CQV lifecycle for process utilities and automation systems (DeltaV, PLC, SCADA) and participate in design reviews to embed CQV considerations from project design.
Job description
Antaes Asia in Singapore seeks a CQV validation engineer with 3+ years in the pharmaceutical industry. You will develop and review commissioning protocols, IQ/OQ/PQ, FAT/SAT, and traceability matrices, ensuring compliance with GMP and CSV requirements.
You will support end-to-end CQV lifecycle for process utilities and automation systems (DeltaV, PLC, SCADA) and participate in design reviews to embed CQV considerations from project design.
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