Experience with metrology equipment for wafer particle inspection, thickness measurement, cleaning, sorting, packaging, and ICP-MS analysis, as well as AMHS equipment such as stockers and Overhead Hoist Transport (OHT) systems, will be an advantage.
Ensure compliance with EHS requirements on work risks and safety precautions, including chemical hazards, working at heights, and maintaining a safe working environment.
You are required to work 12-hour rotating shifts to provide operational support for production activities and ensure timely responses to equipment-related issues in a fast-paced semiconductor manufacturing environment.
Drive Design for Manufacturability (DFM) and Design for Reliability principles, providing expertise in component design, tooling strategies, material selection, and biocompatibility considerations.
Lead process development and validation activities, including DOE, PFMEA, process capability studies, and IQ/OQ/PQ validation, utilizing scientific molding principles.
Ensure compliance with ISO 13485, FDA Quality System requirements, ISO 14971 risk management standards, and other applicable medical device regulations.
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Drive Design for Manufacturability (DFM) and Design for Reliability principles, providing expertise in component design, tooling strategies, material selection, and biocompatibility considerations.
Lead process development and validation activities, including DOE, PFMEA, process capability studies, and IQ/OQ/PQ validation, utilizing scientific molding principles.
Ensure compliance with ISO 13485, FDA Quality System requirements, ISO 14971 risk management standards, and other applicable medical device regulations.
...
Drive Design for Manufacturability (DFM) and Design for Reliability principles, providing expertise in component design, tooling strategies, material selection, and biocompatibility considerations.
Lead process development and validation activities, including DOE, PFMEA, process capability studies, and IQ/OQ/PQ validation, utilizing scientific molding principles.
Ensure compliance with ISO 13485, FDA Quality System requirements, ISO 14971 risk management standards, and other applicable medical device regulations.
...
Prepare and ensure readiness of test bed and test environment to carry out the test execution
Execute test in accordance to the test design/test cases
Analyze test results and work with respective teams to resolve issues such as defect open and resolution rate, bottlenecks in performance and other defects
...
Prepare and ensure readiness of test bed and test environment to carry out the test execution
Execute test in accordance to the test design/test cases
Analyze test results and work with respective teams to resolve issues such as defect open and resolution rate, bottlenecks in performance and other defects
...