.Descripción y detalle de las actividades- Functions as an automation expert and is able to train Automation Engineers (Mechatronics) and Equipment Engineers.- He is an expert and consultant in programming robot arms, vision systems, PLC, HMI and servo motors.- Plans, recommends and executes cost reductions.- Verifies equipment, machinery and tools in automation, making pertinent suggestions in case of improvement possibilities.- Participates actively in the introduction of new automatic processes.- Develops and is highly capable of detailing project work plans including use of Gantts for multiple projects.- Maintains and updates automation project matrices for the entire automation area.- May coordinate groups of Automation Engineers.- Develops work procedures for production equipment and follows up on them.- Quotes and follows up on the purchase (local and foreign) of materials, parts, items, etc., necessary for the completion of projects assigned to him/her.- Maintains documented and updated manufacturing processes, and others that affect the operation of the general activity of the plant.- Participates and acts in the determination of feasibility of automation and semi-automation requests for Engineering requirements (Manufacturing, Quality, NPI, etc.).- Participates and proposes ideas in the design of automation and semi-automation equipment for new or existing products and process improvements.- Analyzes, proposes and makes modifications to the design of existing manufacturing and test equipment in the face of product design changes and or improvements that aid in equipment performance.- Addresses safety issues arising from the design of automatic and semi-automatic manufacturing and test equipment.- Through the use of computer packages (e.G. Solid Works, AutoCAD), prepares dimensional analysis of new equipment for manufacturing and/or testing in order to ensure the correct interaction with the medical products where they are applied.- Support to departments where manufacturing and test equipment presents problems.Experiência y requisitos- Minimum 3 years of verifiable experience in manufacturing processes, preferably in medical devices.- Knowledge in Good Manufacturing Practices and regulations applicable to the medical industry.- In compliance with GMP rules and/or regulations, and all National and International Quality standards according to the Quality Manual.- Professional career in Mechatronics Engineering or related field. Communication and organizational skills. Use of computer packages including Solidworks, AutoCAD, etc. Spoken and written English 90%. Knowledge of Lean Manufacturing, JIT, Kaizen, TPS and Six Sigma production systems