Inspect incoming raw materials and components to ensure compliance with product specifications, particularly ISO13485 and 21 CFR 820.
Perform manufacturing batch record and documentation review for completeness and accuracy prior to product release and/or closure.
Perform environmental monitoring, measurement and publish test report.
Performing physical non-conforming material segregation and disposition per approved instructions.
Perform inventory transactions in JDE as part of quality inspection and product release process.
Maintain filing system for the incoming inspection reports
Requirements
NITEC in engineering or chemical process related disicipline.
1 - 3 years QA experience in clean room environment, preferably in semiconductor / pharmaceutical / biotech industries. Fresh graduates with NTC in Chemical Process Technology can apply.
Ability to read, interpret and understand technical and non-technical supplier control documents including product drawings, specifications.
Able to work 12-hour permanent day shift.
We regret that only shortlisted candidates will be notified.
GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Lim Zi Cheng | Registration No: R2089949
