1 Perform quality control/release testing on products and incoming quality inspections by confirming specifications; conducting visual and measurement tests; rejecting and returning unacceptable materials
2 Perform First Article Inspection (FAI)
3 Perform dimensional & visual inspection of sub-assemblies or final assemblies according to drawings, using gauges and other reliant inspection equipment
4 Perform inspection in accordance with the SFDA, ISO, In-house and other applicable regulations.
5 Approve in-process produced products quantities by confirming specifications; conducting visual and measurement tests; communicating required adjustments to production supervisor.
6 Identify, document, and segregate non-conforming material.
7 Perform finished products inspection by confirming specifications; conducting visual and measurement tests; returning products for re-work; confirming re-work.
8 Document inspection results by completing reports and logs; summarizing re-work and waste; inputting data into quality database.
9 Maintain compliance in a highly regulated environment for medical devices following Good Documentation Practices (GDP)
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To apply, please send your CV to below email address:
[email protected]