Shift QA Lab Analyst PHARMA Up to $3200 #HJN
Summary
Performs quality checks and documentation reviews in a pharmaceutical manufacturing environment, ensuring products meet GMP standards during batch production and release.
Duties:
- Support quality assurance activities including validation, qualification, stability studies, and batch release processes.
- Perform visual inspections of raw materials and finished products to ensure compliance with quality standards.
- Review batch production records, testing documentation, autoclave reports, and quality records for accuracy and completeness.
- Investigate deviations, out-of-specification (OOS) results, and quality issues, and support timely resolution prior to product release.
- Assist in maintaining Quality Management System (QMS) documentation, including SOPs, Master Batch Records (MBRs), forms, templates, and Annual Product Quality Reviews (APQR).
- Conduct in-process quality checks, aseptic audits, line clearance approvals, and support finished goods inspection plans in SAP.
- Monitor KPIs, maintain GMP/GDP compliance, uphold 5S standards, and collaborate with cross-functional teams to support continuous improvement and daily QA operations.
Requirements
- Diploma in Life Sciences, Chemistry, Pharmacy, Biotechnology, Engineering, or a related discipline.
- Experience in Quality Assurance (QA), Quality Control (QC), or GMP-regulated pharmaceutical, biotechnology, medical device, or manufacturing environments.
- Knowledge of GMP, GDP, Quality Management Systems (QMS), batch record review, deviations, OOS investigations, validation, and documentation control and SAP
- Ok with shift work
Janeve
wa.me/6588183965
OR
Email me at janeve.ng@recruitexpress.com.sg
EA Personnel : Janeve Ng Choy Tong
C.E.I: R25159176
Company Registration No: 99C4599
Recruit Express Pte Ltd