Quality Assurance Associate

Job Description: • Contribute to Life Science projects for Antaes Asia clients • Review and verify executed component batch records for accuracy and compliance with GMP/GDP requirements. • Perform timely release of raw materials, buffers, and media in SAP in accordance with approved specifications and procedures. • Support Electronic Batch Record (EBR) review activities for production operations. • Participate in Quality on the Floor (QOTF), GEMBA walks, and provide real-time guidance to operations personnel on documentation practices and GMP compliance. • Assist in identifying and escalating documentation or process deviations during record review or shopfloor interactions. • Collaborate cross-functionally with Production, QC, and Material Management teams to resolve discrepancies or issues related to material release and batch documentation. • Support QA team in continuous improvement initiatives and data gathering for metrics and trend analysis. • Contribute to the promotion of Antaes services on top of assistance provided to clients Job Requirements: • Diploma in Biomedical Engineering, Biotechnology, Life Science or equivalent • 1 - 2 years of Quality Assurance/ Manufacturing within a GMP-regulated biologics or pharmaceutical environment. • Familiarity with Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP). • Exposure to SAP and Veeva Vault would be preferred • Candidate must be highly motivated, be able to work independently as well as in a team and have good organizational and oral and written communication skills • Excellent communication skills, both written and verbal, in English - to liaison with English speaking counterparts