Location: Tuas
Shift Work: Rotating shifts (Mon-Fri)
- 7:00am-3:00pm/3:00pm-11:00pm/ 11:00pm-7:00am
Salary: Up to $2400
Responsibilities
- Review batch production records of critical process steps to ensure batch release criteria are met
- Ensure all deviations are properly investigated and resolved prior to batch release
- Maintain Retention/Reserve Sample Program for whitestocks and finished products
- Coordinate review of alarm reports support investigations and impact assessments for critical alarms
- Assist in preparing and maintaining master documents (SOPs, Forms, Templates, MBRs)
- Support Annual Product Quality Review (APQR) reporting
- Issue Manufacturing Batch Records (MBRs) to align with production schedules and current versions
- Maintain and manage Document Retention Program (archival, retrieval, destruction of quality documents)
- Assist in release of Bill of Materials (BOM) in SAP, ensuring alignment with supporting documentation
- Support supplier quality assurance documentation and filing
Requirements
- Min. Diploma in Life Sciences, Chemistry, Biotechnology or related field
- Meticulous and detail-oriented with strong documentation skills
- Willing to work on rotating shifts
- Prior experience in QA/QC or regulated manufacturing (e.g., pharmaceutical, medical device) is a plus
- Good understanding of GMP and regulatory compliance preferred
If interested, please email me at [Confidential Information] or telegram @fullviana
Alex Goh Hock Leong
(CEI.No: R1763413 l Recruit Express Pte Ltd (Healthcare & Life Science) | 99C4599).
