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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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.
OR related field AND 2+ years software industry experience in system testing (involving networking / storage / virutalization product line) with coding in languages including, but not limited to, C, C++, C#, or Python.
OR Master's Degree in Engineering, Computer Science, or related field AND 2+ years technical engineering experience with coding in languages including, but not limited to, C, C++, C#, or Python.
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.
...