-Inspect incoming raw materials and components to ensure compliance with quality specifications, particularly ISO 13485 and FDA 21 CFR part 820.

-Perform inspection, manufacturing batch record and documentation review for completeness and accuracy prior to product release and/or closure

-Perform physical Nonconforming 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 inspection reports.

-Assist in trending of quality data, monitoring and report on quality procedural deviations.

-Interact and co-ordinate with other departments to resolve quality issues.

-Participate in quality and process improvement opportunities

Requirements :

• Minimum ITE or equivalent.
• 1 - 3 years QA experience in cleanroom environment, preferably in semiconductor / pharmaceutical / biotech industries. Fresh graduates with NTC in Chemical Process Technology can apply