Position Description Assists with qualification process; troubleshoot any equipment malfunction; set-up and fine-tune equipment. Adjusts equipment setting in order to build samples as per Experiment's Design, or qualification/validation plans. Conducts any testing and take measurements as required in the plan. Properly documents activities and record test results. Provides direct support to the production line and operators. Monitors process and equipment performance and takes preventive action. Partners with Engineers, Quality, and Production personnel to quickly contain and prevent any quality related issues. Evaluates potential nonconforming product. Under the guidance of Manufacturing Engineers, participates on equipment Buy-Off activities, performs initial equipment installation and qualification, prepares list of spare parts, and defines PM procedures and frequency. Trains line technicians on equipment functionality, and PM procedures. Physically arranges and moves workstations and equipments as per the latest Layout plan. Assists engineers in implementing ECOs. Prepares technical reports as required. Position Responsibilities Provides engineering support to the manufacturing line. Updates/ revises existing manufacturing procedures. Assists in product or technology transfers. Coordinates custom development builds. Provides traceability documentation for engineering builds. Conducts experiments / tests for engineer. Collects and analyzes numeric data. Assists in the adequate disposition to non-conforming product/material (P.R.B./M.R.B.) Performs other position duties as assigned Quality Responsibilities Reports any observed or informed process and/or product non-conformities to the Supervisor. Finds resolution of Quality Situations at the area of responsibility. Reports any complaint regarding a Medtronic product to the Supervisor. Complies with all the requirements in the operational procedures at the area of responsibility in order to meet the requirements of all applicable Quality System Regulations (e.g.: FDA Part 820 Quality System Regulation, ISO 13485 Quality Standard, R-PAL (Japanese QSR's). EHS Responsibilities Acknowledge and maintain commitment with the EHS Policy Participate in the development of EHS improvement projects Participate actively in the EHS programs to achieve the objectives and targets defined for the area Minimum Education Associate Degree or 60 undergraduate approved credits as equivalent Basic Qualifications Background Educational: Electronics, Engineering Technology, Industrial Technology or related field Experience: o Senior Level: 5 Years with Associates or 3 Years with Bachelors Able to read schematics and have an understanding of analog and digital circuits, Operate test equipment and Soldering experience Skills Analytical Thinking Problem Solving Interpersonal Relations Quality and Results Oriented Computer Literate Basic oral and written communication skills in Spanish and English Desired/ Preferred Qualifications Background Experience in medical device, pharmaceutical, or electronic industry Experience in PLC, Robotics, Motion Control and Vision Systems Skills Teamwork Communications Continues Improvement Project Management Good Mechanical Skills, use of small hand tools. Advance oral and written communication skills in Spanish and English Working Conditions Mental Components: Capacity to calculate, classify, compare, coordinate, copy, edit, evaluate, interview, instruct, read, observe, organize, plan, compile, select, request and document. Physical Components: Light work requiring physical effort, in addition, requires communication skills, capability to move from one place to another, visual discrimination and tolerance to the use of personal protection equipment. Environmental Work is performed in building's interior with normal temperature, good illumination, air condition, clean environment and minimum risk SDL2017
