Basic UP $5000 (With Relavant Exp in Electronics Manufacturing)
5 days (Office hour)
Serangoon
Your Responsibilities: -
Manage and oversee quality audits by plan and ensure quality audits are rectified and implemented.
Support and improve ISO13485, ISO14971 and FDA 21 CFR Part 820 systems and provide awareness training on the ISO.
Coordinate and assist on external audit such as Customer, ISO certification and Regulatory bodies.
Ensure the procedures and processess are implemented as per perscribed by the Quality Management System.
You will need: -
At least 2 years of relevant QA experience in electronics manufacturing / medical device manufacturing
Have an excellent knowledge of Quality Management System primarily in ISO 13485, ISO14971 and FDA 21 CFR Part 820.
Diploma in Quality Engineering or equivalent
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