AMARIS ACT PTE. LTD. in Singapore is looking for a MES Validation Engineer to support validation activities for Electronic Batch Record (EBR) systems within a GMP-regulated manufacturing environment. The role requires reviewing validation documentation, supporting MES testing activities, and ensuring compliance with GMP, GDP, and data integrity standards.

The ideal candidate holds a Bachelor’s degree and has 5-7 years of experience in MES validation within pharmaceutical environments. The position emphasizes collaboration with Manufacturing, Validation, and IT teams to ensure proper documentation and audit readiness.