QC Analyst: GMP Lab Ops & Method Validation

No deviation Pte Ltd. in Singapore is seeking QC Personnel to support Quality Control laboratory activities. This role involves hands-on experience with laboratory systems such as GLIMS, Veeva, and SAP, ensuring compliance with GMP requirements.

The ideal candidate has 2 to 5 years of QC laboratory experience, particularly in a pharmaceutical setting, and is capable of performing routine testing and supporting method validation activities.