Serve as focal point of contact for customers on quality-related matters with minimal supervision.2. Ensure products meet customer specifications, drawings, and quality standards.3. Lead customer audits preparation, coordination, and follow-up on audit findings.4. Lead root cause analysis and corrective action implementation; ensure timely closure and effectiveness verification.5. Prepare and maintain quality documentation (Control Plan, Inspection Reports, FAI, PPAP documents where applicable).6. Monitor quality performance metrics and drive improvement actions based on data analysis.7. Identify process improvement opportunities and work with cross-functional teams to implement solutions.8. Provide technical guidance to QA Technicians on inspection methods and quality requirements.9. Participate in new product introduction (NPI), including pretest, first article inspection, and buyoff.10. Support QMS implementation, audit compliance, and continuous improvement initiatives.11. Handle internal non-conformance and support MRB activities.12. Ensure compliance to ISO standards, safety practices, SOP, and company policies.13. Mentor and coach E1 on quality standards and documentation best practices.
Demonstrates strong attention to detail and precision in selecting specifications and executing measurements in accordance with correct CD definitions. Familiarity with process layer structures (e.g., nitride, spacer) is an added advantage.
Shows patience and consistency in performing repetitive measurement tasks.
Possesses strong analytical thinking, including sound decision-making on whether CDs should be corrected or retained. Able to assess if available specifications provide sufficient information to proceed with CD corrections.
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Demonstrates strong attention to detail and precision in selecting specifications and executing measurements in accordance with correct CD definitions. Familiarity with process layer structures (e.g., nitride, spacer) is an added advantage.
Shows patience and consistency in performing repetitive measurement tasks.
Possesses strong analytical thinking, including sound decision-making on whether CDs should be corrected or retained. Able to assess if available specifications provide sufficient information to proceed with CD corrections.
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Oversee and manage all QA aspects from NPI stage till mass production.
Lead APQP activities, ensuring all phases are properly executed and documented.
Collaborate with cross-functional teams including R&D, Manufacturing, Engineering, and Supply Chain to ensure quality requirements are met throughout the product life cycle.
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Conduct inspection on returned FG (Media, Bag, Carton, or Pallet) and ad-hoc impacted FG, with accurate disposition and documentation per quality standards.
Perform Out-of-Box (OBA) Audits on FG to verify packaging integrity, labeling, and product conformance prior to shipment.
Execute FG Archive activities per established retention and traceability procedures.
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Participate in Non-conformance issue part containment and disposition discussion, and execution during quality incident.
Responsible for review and approval of discrepant lot disposition in eNCS. Hold authority to reject in the system if it does not meet release requirements.
Lead Material Review Board (MRB) for Part Containment and Disposition.
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Oversee and manage all QA aspects of NPI (New Product Introduction) projects from concept through to mass production.
Lead APQP activities, ensuring all phases are properly executed and documented.
Collaborate with cross-functional teams including R&D, Manufacturing, Engineering, and Supply Chain to ensure quality requirements are met throughout the product life cycle.
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Conduct inspection on returned FG (Media, Bag, Carton, or Pallet) and ad-hoc impacted FG, with accurate disposition and documentation per quality standards.
Perform Out-of-Box (OBA) Audits on FG to verify packaging integrity, labeling, and product conformance prior to shipment.
Execute FG Archive activities per established retention and traceability procedures.
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WD thrives on the power and potential of diversity. As a global company, we believe the most effective way to embrace the diversity of our customers and communities is to mirror it from within. We believe the fusion of various perspectives results in the best outcomes for our employees, our company, our customers, and the world around us. We are committed to an inclusive environment where every individual can thrive through a sense of belonging, respect and contribution.
Conduct inspection on returned FG (Media, Bag, Carton, or Pallet) and ad-hoc impacted FG, with accurate disposition and documentation per quality standards.
Perform Out-of-Box (OBA) Audits on FG to verify packaging integrity, labeling, and product conformance prior to shipment.
Execute FG Archive activities per established retention and traceability procedures.
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Equipment Operation & Maintenance: Proficiently operate ICT testing machines, functional test fixtures, and automated testing equipment. Perform daily inspections and basic preventive maintenance.
Product Testing: Execute testing procedures according to work instructions and accurately determine test results as “Pass” or “Fail.”
Initial Troubleshooting: Conduct preliminary analysis on failed products to identify whether issues are caused by product defects or testing equipment/program problems, and report according to established procedures.
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Identify, coordinate, and monitor the implementation of quality and process improvement initiatives in collaboration with key stakeholders to improve processes, enhance patient safety, and ensure compliance with applicable regulatory and accreditation requirements.
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