CQV Validation Engineer – GMP Pharma Facilities

JDA WMS PTE. LTD. is seeking a Validation Engineer in Singapore to drive CQV activities for GMP-regulated pharma and biopharma projects.

You will validate equipment, utilities, and systems, prepare validation documentation, and ensure compliance with GMP, GAMP 5, and FDA 21 CFR Part 11. You will coordinate with project engineers, QA, clients, contractors, and vendors, perform risk assessments, CAPA, and support FAT/SAT during commissioning.