● Responsible for managing and ensuring the Quality Management System, ensuring compliance with the rules and regulations applicable to the IATF customers, developing, documents, and trains updates or changes in applicable regulations. ● Responsible for leading internal, external and client audits, following up on the results of these. ● Verify each document change ensuring that document changes or registrations do not affect compliance with applicable IATF and customer specific requirement and regulations. ● Ensuring documentation risk management, being updated in interacting with project team members including engineers, managers. ● Evaluate procedures within the quality system to identify areas for improvement. ● Participate in meetings for department goals and objectives. ● (KPI) Support to new project requirements such as validations and CQI-17 audits, ensuring compliance with regulatory requirements. ● My main contributions were letter of conformity IATF TUV certification.

● Responsible for field containment and rework activities at customer locations, such as product diagnostic tests, assembly line investigations, support and maintain practices related to manufacturing support of issues at customer assembly plants and quality situations related to product application, analyze, compile, review and regularly report customer quality metrics such as PPM, for performance. ● Prepare presentations from quality data for reviews by both Corporative and customer management groups. ● Obtain customer approvals for manufacturing process change(s) by providing supporting data for the change(s) and submitting to customer in their required format. ● Lead problem analysis and improvement efforts by applying the use of modern quality tools such as FMEA, 8D, 5 why. ● Ensure information flow related to customer returns to appropriately address, facilitate awareness of issues and deploy countermeasures as lessons learned. ● Assist internal and external contacts to resolve product and process problems. ● Investigate and solve manufacturing-related problems. ● Continuous communication with design and engineering team during early and launch stages and also leader for Root Cause analysis and PCAs for Launch issues. ● Interface with Engineering and Operations to ensure transfer to Production of new products are in accordance with approved data. ● Assure customer specific requirements are implemented. ● PPAP or any other customer approval documentation for new products. ● Safe lunch Plan coordination activities.

● Coordinate internal and external audits of the QMS, or of the client (if applicable). ● Follow-up of non-conformities related to the QMS (internalexternal) or of the client, coordinate and supervising the process of control of records and procedures to adhere to the revisions and requirements of the standard or the client. ● Ensure that the client's requirements are included in the procedures and documents that apply, coordinate and follow up on the corporate requirements that apply to the QMS, problem solving tools and quality control systems and procedures (IATF 16949). ● My main achievement is monitoring and closure of corrective actions and evidence on the IATF portal, period 2021 of 18 non-conformities 3 major non-conformities and 15 minor non-conformities. ● IATF certification period August 2022 IATF with only three minor noncompliances. ● 100% compliance with the internal audit program, period 2021-2023.

● Responsible to track and locate the failed components in the data centers to import and logistic the material, to locate them in the internal laboratories, generate work orders with the reworked components in order to make controlled ORT RTD runs. ● For the follow-up of the failures with the team of FAE and repair, meetings with the customer to follow up the fails and disposition of the material, management of personnel with a total of 12 quality inspectors, (4 per turn) and 2 jr engineer. ● My main contributions were reduction in laboratory repair time, reduction in customer failure reports, increased shipments of controlled orders.

● Responsible to follow up inspection plans for raw material & Customer Impacts. ● Review and disposition of suspect material. ● Rejection areas audits and RMA process, corrective actions follow up and verify, monitors. ● Approves and shares documents review, under the updated revision in line with standards, Quality Management System and/or customer requirements. ● Ensures received raw materials, semi-finished and finished goods conformity in accordance with control plans and procedures, monitors incoming non-conformity management, suppliers claim and quality performance. ● Manages process parameters deviations, oversees the application of control plans, methods and instructions for measuring and monitoring manufactured cables characteristics during all the different steps of production. ● Follows up, product control results, product transfer for rework process. ● Manages deviation requests, elaborate supplier's claims management process by ensuring supplier audits and visits. ● Elaborate in time of 8D reports and/or presentation including root causes analysis and finalized actions plan in order to guarantee high level of customer satisfaction. ● Communicates supplier assessment results to concerned parts and assures effective and proactive customer support for problem solving and improvement proposal.

● Responsible to support during the NPI phase, documentation for PPAP, FMEA, PCP, process and product audits, coordination of meetings for the implementation of engineering changes, lead the solution of quality problems. ● Verification and calibration of measuring equipment of the plant, communication with the customer, management of personnel with a total of 54 quality inspectors, (18 per turn) and 3 quality leaders. ● My main contributions were reduction of level change times (engineering changes), reduction of line validation times. ● ISO TS 16949 certification.

● Responsible to validation of measurement equipment and instruments, prototypes, statistical analysis of capacity, preparation of PFMEA's, PPAP, PCP, preparation of documentation (work instructions, engineering changes, procedures, CAPA actions. ● Management of personnel with a total of 35 quality inspectors, (7 per turn) and 5 quality leaders. first, second, third and weekend shifts. ● My main Contribution was the reduction of material for rework, reduction in sample validation delivery times, 100% compliance with the internal and external calibration program.

● Responsible to coordination of internal audits, inspection of first samples, logistics, manufacturing and quality procedures, preventive and corrective actions (CAPA). ● Identification and prevention of problems, implementation and maintenance of QMS, management of personnel with a total of 9 quality inspectors, (3 per turn) and 3 quality leaders. ● My main contribution was material reduction of rework. ● Reduction of internal PPM's, follow-up and timely closure of internal corrective actions, 100% compliance with the internal audit calendar.