For Employers
Quality Assurance Associate


ANTAES ASIA PTE. LTD.
a day ago
Posted date
a day ago
N/A
Minimum level
N/A
Full-timeEmployment type
Full-time
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
Related tags
-
JOB SUMMARY
Quality Assurance Associate
ANTAES ASIA PTE. LTD.
Singapore
a day ago
N/A
Full-time

Quality Assurance Associate