Responsible for Engineering Change Review, 8D Review, and coordination, interface with downstream as required, e.g., excursion-related, packaging feedback.
Responsible for following up and following through on committed actions/evaluation lots for improvements.
Participate in related risk assessment activities and improvement activities with relevant parties as applicable, e.g., HIRADC, EIA, ROA, FMEA, CI.
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Able to manage routine laboratory analysis and urgent/ad-hoc failure cases with minimal supervision, ensuring timely completion of investigations and reports.
Capable of working independently to conduct detailed failure investigations while also collaborating effectively with engineering, quality, and production teams to resolve issues.
Proficient in written and spoken English to clearly document analysis findings, prepare technical reports, and communicate results and recommendations to cross-functional teams.
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Identify defects such as cold solder joints, bridging, lifted pads, or misalignment
Perform functional checks or assist in validation testing after rework
Carry out additional rework tasks such as liquid masking, stuffing PCBAs, lead trimming, masking/unmasking, manual cleaning, repair damaged PCB traces, and mechanical assembly.
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Provide guidance and advise on best industrial practices related to quality, environmental, occupational health & safety, and document control systems.
Support company initiatives related to QMS, EOHSMS, compliance, and operational excellence.
Prepare, review, revise, and maintain internal and external controlled documents including procedures, work instructions, forms, manuals, templates, and related documentation.
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Responsible for the qualification of new tools, processes, and products. This includes conducting incoming inspections, accepting newly fabricated tools and related hardware, and setting up and operating processes and equipment required to generate qualified products.
Where applicable, responsible for verifying, filing, compilation and documentation of test reports, test results in SAP, relevant documentation of all tests/inspections conducted, quality batch records and final release report.
Immediate verification upon out of specification test results with superior to confirm the product failure or test deviation.
Where applicable, perform results recording and/or stock transactions in SAP.
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