Wilson Leong

Wilson Leong

Quality Assurance Engineering Assistant

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  • Timeline

  • About me

    Quality Engineering Manager at Ascensia Diabetes Care

  • Education

    • University of London

      2000 - 2004
      Degree Information Systems and Management 2nd Class Lower Honors
    • Queenstown Secondary School

      1989 - 1994
      O Levels English, Chinese, Mathematics, Geography, Physics, Chemistry, Design & Technology
    • Temasek Polytechnic

      1995 - 1998
      Diploma in Quality Engineering Quality

      Quality Engineering

    • River Valley Primary School

      1982 - 1988
      PSLE English, Chinese, Mathamatics, Science
  • Experience

    • Coilcraft Industries Singapore Pte Ltd

      Dec 2000 - Sept 2002
      Quality Assurance Engineering Assistant

      Conduct periodic calibration of equipment and aquire secondary dependance of external calibration vendors to facilitate comparsion of vendors to choose from at company's advantage.Conduct periodic correlation of production chip inductors against Master correlations to ensure they fall within specific acceptance tolerances.Conduct periodic internal audits of the company and submit report upon each audit in preparation for the company next upcoming external auditing of QS9000.

    • Maxtor Peripherials Singapore Pte Ltd

      Oct 2002 - Sept 2006
      Quality Assurance Realiability Associate Engineer

      Update and analyze realibility issues of products and follow-up any discrepancies found.Coordination with various departments for weekly scheduled tests and reports of products.Overseas transition/training at Shrewbury Massachusetts in United States for 3 months.Engineering/Design verification of new release of product qualification.Development/Revision of software systems to improve work process/productivity.Support troubeshooting of testers (Flexstar/Xyratex) software and hardware system. عرض أقل

    • Flextronics Manufacturing Singapore Pte Ltd

      Jan 2007 - Aug 2008
      Supplier Quality Engineer

      Coordinate and resolve quality issues from Incoming to manufacturing operations on its disposition (Use-as-it-is, Waiver, Rework, Scrap or Return to Vendor).Schedule/Ad-hoc audits on suppliers' quality process and documentation to meet company's quality expectations and standards.Review and compile quality records and documents of suppliers for management review on their quality performance and expectations.Initiate the project for segregation of both local and overseas suppliers backlog rejects for further evaluation b the suppliers' on its disposition. Implementation saves up to US$300,000 anually for the company عرض أقل

    • Bio-Rad Laboratories Singapore Pte Ltd

      Aug 2008 - Sept 2011
      Supplier Quality Engineer

      Investigating, analyzing and correcting problems in quality, production and control of quality issues from company to suppliers.Managing and monitoring of in-house quality and suppliers on quality improvement and performance.Perform and coordinate First Article Inspection.Conducting Internal audits in company on ISO9001 and/or ISO13485.Audit Lead in both local and overseas suppliers’ quality management system on ISO9001 and/or ISO13485.

    • Waters Pacific Pte Ltd

      Sept 2011 - Oct 2015
      Supplier Quality Engineer

      Support Product Transfers and New Product Introduction (NPI).Supplier audit of Contract Manufacturers and Key suppliers.Drive and approval of First Article localization activities with Asia suppliers.Identify and define supplier quality expectations with Contract Manufacturers and Asia suppliers.Drive resolution of part quality issues with suppliers and collaborate with the Manufacturing Engineering to implement corrective actions.Perform periodic supplier audits for both local and overseas.Drive/Support development of new methodology, processes and product design into the contract manufacturers and supply base.Support and management of the company's Quality Management System. عرض أقل

    • Hill-Rom

      Nov 2015 - now
      Senior Supplier Quality Engineer

      Quality Lead for New Product Development (NPD) projects and Sustaining projects for Respiratory Care products.Develop, implement, and monitor early supplier quality development initiatives, including supplier performance management, supplier certification, process improvements, supplier quality audits and supplier selection activities.Develop Quality Plans and provide quality support for new product introduction (SNAP and FAI activities).Execute contracts and Quality Plans with suppliers to ensure quality requirements are consistently achieved.Drive Global Supplier Quality Metric review and discussion through the Global Supplier Quality Council.Develop and drive supplier assessment/improvement, supplier audit schedule, supplier scorecard, supplier corrective actions, and qualification / disqualification of suppliers.Ensure supplier compliance to REACH, RoHS, Conflict Minerals, and other international standards involving suppliers.Involvement in various continuous improvement/process improvement teams.Develop, modify, or review for approval any procedure related to product development. عرض أقل

    • Ascensia Diabetes Care

      Feb 2019 - now
      Quality Engineering Manager

      Supplier quality lead of New Product Development projects and sustaining projects for Blood Glucose Monitor (BGM) & Continuous Glucose Monitoring (CGM) products.Lead, improve and maintain Supplier Quality Management (SQM) processes in the APAC, including assigned global region and alliance partners.Direct quality interface to internal team and suppliers/service providers supporting quality and productivity goals, monitoring and measuring product/process quality performance trends and troubleshooting of production/release issues.Establish and maintain quality plans and/or agreements with suppliers/service providers in both quality and regulatory compliance of the product/service and customer expectations.Represent Quality in Product Lifecycle Management (PLM) teams, New Product Development (NPD) Element teams and other project teams in developing and implementing Supplier Quality Plan and/or Supplier Development Plan (SQP/SDP).Review and approval of product/process change or deviation from suppliers/service providers and within the company.Internal and supplier/service provider audits, including supporting role from health authorities/regulatory agencies.Optimize Standard Operation Procedures (SOPs) and support Global Supplier Quality process improvements. عرض أقل

  • Licenses & Certifications

    • ISO 13485 Lead Auditor

      SGS
    • ISO 27001 Lead Auditor

      BSI Training Academy