Participate in design reviews, training and continuous improvement initiatives to enhance overall processes
Assist Process development activities (Process parameters scouting, optimisation, verification and Process Freeze) in Development projects to meet the project targets in term of timeline, quality, cost competitive and manufacturability.
Generate and update relevant documents, eg Process Specification, PFMEA,DFMEA, Master FMEA, OJTI, T32, PDR
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Lead cross-functional quality and improvement initiatives, including FPY improvement, external quality issues, warranty and failure analysis, MRB/ECB participation, and corrective actions.
Support continuous improvement and life cycle activities such as VAVE, process yield improvement, vendor and part qualification, and collaboration with R&D, RAQA, Supply Chain, and Manufacturing.
Diploma or Bachelor’s Degree in Engineering (Mechatronics, Electrical/Electronics, Mechanical, Industrial, Production, or related discipline).
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Design and develop semiconductor components, tooling, and related parts to deliver robust and compliant solutions.
Create and review detailed 2D/3D CAD models, drawings, specifications, and schematics to meet performance, quality, cost, and schedule requirements.
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Prior Exposure to Biopharma projects is advantageous
Lead process systems from conceptual design through detailed design, construction, commissioning, and final handover.
Develop and progress key design deliverables, including PFDs, P&IDs, specifications, datasheets, and functional descriptions in line with project requirements.
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Collaborate with Equipment Engineers to drive yield, quality, and throughput improvement projects.
Work with cross-functional teams to implement corrective actions on quality-related issues.
Partner with external vendors to identify root causes, provide application support, and address topics relevant to the smooth operation of manufacturing equipment.
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Coordinates company technical projects with subcontractor and is the point of contact for design review, project timeline, characterization requirements, qualification progress and internal/external documentations readiness.
Ensure smooth transition of qualified device/package from qualification stage through high volume manufacturing (HVM) by upfront effective risk assessment to mitigate potential risk from assembly characterization, risk build and initial production release.
Develops, deliver technical presentations and design generation required for project launch, execution till implementation.
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