Manimaran Chellaperumal

This is Manimaran Chellaperumal, Working as Associate Engineer in Sanmina-SCI Singapore Pte Ltd from 2018 to till date. I am looking job change to India in Quality Department.

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.

Diploma in Mechanical Engineering – Nanjappa Institute of Technology (2002 – 2005)

S.S.L.C – New River Matriculation Hr.Sec.School (2002-04)