Experience

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  Pall corporation

  Aug 1999 - Mar 2006

  Fabrication machine operator, level 2

  • Responsible for operating a PLC interface equipment.• Additional responsibilities include basic repairs, preventive maintenance.• Verified all settings of the tool with QA prior to run.• Understood and communicated important issues to the Supervisor in a timely fashion.• Responsible for Line Clearance prior to run different products or Change Over.• Ordered more parts/materials from the warehouse if needed.• Return To Stocks the left over materials to the warehouse at the end of the shift. Show less

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  Siimpel corporation

  Apr 2006 - Feb 2014

  Wafer fab technician, level 2

  • Responsible for supporting micro-electro-mechanical systems advanced process engineering; processes include photolithography, wet etching, metal deposition, Ag paste dispensing and dry etching on 6, and 8 inch bare silicon and SOI (silicon on insulator) wafers. Tools used include: Primaxx wet/dry etch HF tool, HMDS Oven, Karl Suss RC8 Spinner, Karl Suss MA6 Contact Aligner, Anatech 600 Series Plasma Asher, STS DRIE, Unaxis 790 Series RIE, Temescal E-Beam Evaporator, Tystar Furnace, GPD dispenser, Essemtec PnP Tool, and Denton Vacuum Desk II Deposition System. • Characterize wafers in-process and upon completion using a variety of metrology tools. JEOL SEM, Tencor Alpha Step Profilometer, Nanometrics 210 Film Thickness System, FilmTek Film Thickness System, Tamar wafer thickness, Resistance Probe Station, and McBain Microscope with Measurement Capability. • Assembly and disassembly electro-mechanical systems in process and automation facility.• Maintain and follow clean room and wafer protocols. Show less

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  Posey company

  Mar 2014 - Jul 2019

  • Perform root cause analysis to the component level for complaints related to electronic devices, including invasive and destructive testing, accurate conveyance of the results, early escalation of potential product problems, and researching and suggesting design changes to improve product performance, safety and effectiveness. • Own Corrective and Preventive Actions (CAPA) related to product defects and deficiencies in the Quality Management System (QMS). Successfully led a CAPA that reduced the number incoming inspection nonconformances related to a Class II medical device by 80%.• Using industry best practices, created data analytics to measure Defects per Million Opportunities (DPMO) and Sigma Levels to identify opportunities for process and product improvements. • Link post market data analysis with design and process risk management to ensure a closed loop risk management system. • Interface with Quality/Regulatory to ensure accurate conveyance of evaluation results in order to achieve accurate reportability decisions and timely submission of Medical Device Reports (MDRs) and Adverse Event Reports.• Assist with new product development, including providing design inputs based on the pre- and post-market experience with similar devices, as well as assisting with the development and execution of design verification and validation.• Assist with the development and execution of software validations related to product development, as well as off-the-shelf software validation related to any software used in the execution or maintenance of the QMS. • Reduced the amount of time necessary to investigate complaint products from an average of fourteen (14) days to an average of two (2) days while also increasing the level of investigation and thoroughness of the documentation. Maintained this performance by completing over 99% of device investigations on target. Show less • Responsible for the inspection, evaluation and/or investigation of product related to complaints, service and/or quality assurance initiatives.• Perform hands-on troubleshooting of basic electrical and mechanical functions, assesses failure condition, failure mode in accordance with established procedures and/or under the guidance of Engineering/Quality Engineers or other Quality Management.• Responsible for generating accurate and timely data and reports of results.• Work with other members of the product surveillance team and other functions to ensure timely, appropriate complaint handling and adverse event reporting.• All other duties as assigned by the Manager to meet company objectives. Show less

  • Quality Test Engineer

    Dec 2015 - Jul 2019

  • Associate Quality Engineer

    Mar 2014 - Dec 2015
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  Tidi products

  Jul 2019 - now

  • Senior System Administrator

    Jan 2024 - now

  • Sr. Post Market Surveillance Engineer

    Jul 2019 - Mar 2024