Engineering Assistant at SANMINA-SCI SYSTEMS SINGAPORE Pte Ltd. (2018-05 – Present)
- Reviewing Manual and Electronic Device History Record for a finished product of ICQ Instruments, SCM, KITS and ACP Spares of ABBOTT Products.
- Closing CCNs with proper explanations.
- Preparing PFMEA and PCP, Supporting to Engineers in Critical and urgency situations.
- Prepareing COC for finished products.
- Supporting Philips, Abbott-HSQ, ICQ, ACP.
- Support PQE on product quality issues, including submission of regular quality reports.
- Support the team on eNCMR implementation
- Support First Pass Yield Improvement.
- Successfully achieved a Manual reprocessing report to eReprocessing Report.
- Physical Inspection on Sub-Assemblies and regular Production line Auditing.
- Completed training for an understanding of ISO13485:2003&EN ISO 13485:2012 Medical Devices-Quality Management Systems-Requirement for Regulatory Purposes.
- Performing in-process Audit on manufacturing line to ensure Good Manufacturing Practice and Quality on Product.
- Ensured that Quality Assurance standards were maintained throughout a product life cycle.
- Monitored facility and implemented Quality systems for products in accordance to cGMP and ISO standards.
- Responsible for Continual improvement activities to enhance the products and the environment; through training and work instructions.
- Documented process and prepared reports to be presented in technical presentations.
- Coordinated with the operations department and ensured that new products were produced in accordance to procedures.
- Find the issue and Support to Raise NCRs for wrong documenting's
- Control the GDP and ensure the process to meet the Customer Expectation.
- Perform baseline audit once in a week to reduce the Major errors to Achieve Monthly OTD.
- Trained junior staff department in implementations of various quality tools and procedures.
Assistant Engineer at Intec solutions (2015-09 – 2018-04)
- Ensure process operation is running under standard operation conditions
- After Troubleshooting need to prepare Trouble Report and to be attached with the Daily Production Report, Also monitoring long term troubles and doing counter measures.
- Doing Daily & Weekly Maintenance & Preventive maintenance activities.
- Prepare raw material collection
- Equipment Calibration
- Keep 5's in proper.
- Ensure the machine parameter during setup and troubleshooting for the different kinds of packages as per specification
- Online Monitoring to improve the Equipment efficiency and lead the setup team
- Ensuring Preventive and safety measures in the department
- Repaired and modified existing equipments
- Breakdown and Preventive Maintenance of Auto Screwing machines
- Preparation of Material list and Maintenance checklist
- Good understand work hazards, safety practices, mechanical operating configuration, and policies and procedures
- Responsible for all audit documentations and facing the audit
Quality Assurance Technician at Flextronics Manufacturing Engg Pte Ltd. (2011-07 – 2015-06)
- Inspect the Medical Instruments as per customer given specs.
- Final Inspection the all sub-assemblies in the Production area, Syringe, ITV, Instrument Pumps & Installation Kits for the Finished goods Machines.
- ABBOTT is the one of the main customer of us.
- Inspect the Advanced Blood checkup Machines - I1000sr, I2000sr – Blood Checkup Instruments.
- Final Inspection of RSH – Robotic Sample Handler Instruments.
- Manual inspection of the all Medical Instruments Device History Record, before submitting to the QA Engineer.
- Final Checking the Edhr – Electronic device History Record documents before submitting to the ABBOTT Customer.
- Responsible for the Final Quality Audit & out of Box Audit for the finished goods.
- Direct Discussions to the ABBOTT Quality Manager about the NCMR.
- Coordinate the work of consultant engineers, developers to recommend corrective actions as needed.
- Inspecting the ACP (Accessories Catalog Part) project of ABBOTT, HEMATOLOGY. Online inspections, Study the VMI – Video Manufacturing Instruction. Verify the Current Revision with Production Building lot.
- Scanning & merging the documents for the customer review.
- Prepare and deliver oral and written reports and presentations to the ABBOTT Customer.
- Having experience in PI Auditing.
QC Technician at Softronics (2008-01 – 2011-06)
- Assigned the tasks of conducting quality testing and evaluating the results with the help of supervisors
- Responsible for generating Quality Assurance Programs for trainees to maintain the standard of testing
- Handled the tasks of monitoring and supervising production policies and activities to ensure compliance with the guidelines of quality control
- Assigned the tasks of documenting conducted tests on production line
- Responsible for updating the results of Quality Assurance testing to production supervisor
- Ensured that quality assurance inspections are completed in a proper manner
- Handled the tasks of providing assistance to QA departments to ensure compliance with the quality standards of the organization
- Responsible for monitoring production testing to identify major problems
- Maintained technical files and documents to establish quality standards throughout the production line
Final Inspector in Quality Assurance at MICROCIRCUIT TECHNOLOGIES SINGAPORE PTE LTD (2008-07 – 2008-12)
- Inspect the microchip board through the smart scope
- Well experience having to run the final clean conveyor machine for cleaning purpose of microchip panel board.
- Having good experience in different kinds of panel board cleaning.
- Control the scrap through the final clean machine List.
- Report to the supervisor for the rejects.
Quality In charge at MACRO DISC (2006-05 – 2008-06)
- Responsible for New R&D Products Inspection
- Responsible for Project department Instruments Calibration & Records.
- Responsible for Training of Project department activities
- Preparation of Weekly and Monthly Project department reports & charts
- Handled customer queries to meet their expectations
- Assisted process quality branch in terms of development and quality control plans.
Quality Controller at RUPI ELECTRONIX (2005-06 – 2006-04)
- Perform extensive re-testing on scanners, software, and related components, as well as out-of box units, to ensure specifications are properly met i.e., functionality, free of defects, and properly labeled.
- Monitor Assemblers to ensure units are assembled according to specs on In-Process check list.
- Observe working area (twice weekly) for violation of rules as indicated on the Procedure Report.
- Issuing the parts to concern departments.
- Inspecting the received materials whether checked or not.
- Analyzing the customer reports.
- Observing the faults.
- Take immediate corrective action: put units on hold, notify supervisor and process necessary paperwork.
