**We are searching for the best talent for Principal Manufacturing Systems Engineering Technician to be in Juarez.****Purpose**:**You will be responsible for**:Under limited supervision and in accordance with all federal, state and local laws/regulations and procedures and guidelines of the Johnson & Johnson Corporation, this position:- Participates in the administration and configuration of MES systems.- Coordinate and deliver training to MES users.- It provides support in the development, testing, validation and implementation of configurations of such systems.- It provides support in the process of deploying the MES system to production, in aspects such as documentation, training of production personnel and problem solving in the same area.- Participates in the modification and maintenance of guidelines and procedures related to the areas of responsibility.- Participates in the discussion of conceptual bases for the design and development of new configurations of manufacturing systems.- Responsible for monitoring Interfaces related to the MES system.- Participates in non-conformities of quality.- Collaborates in CAPA actions related to the MES system.- Responsible for communicating business-related issues or opportunities to the next administrative level.- Responsible for ensuring that subordinates follow all of the Company's guidelines related to Health, Safety and Environmental practices and that all necessary resources to do so are available and in good condition.- Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies and procedures.- Perform other assigned tasks as needed.**Calificaciones** Qualifications and requirements**- Studies in Technical Career or equivalent applicable to the area: Mechanical; Electrical; Electromechanical; Electronic; Metrology; Instrumentalist or system preferably.- 6- 8 years of experience and/ or related training preferably.- Knowledge and Skills to successfully develop the responsibilities of the position.- Extensive knowledge in computational packages.- Bilingual: Spanish/English preferred.- Knowledge of GMP's (Good Manufacturing Practices) / ISO preferably.- Knowledge in process/product/SDLC validation activities).- Knowledge of FDA regulations 21-CFR part 820 (Preferably).- Basic ability to read and understand technical documentation associated with the specific discipline.- Knowledge of JDE, CMMS and cPDM (Preferably).- Knowledge in Engineering Changes ECOs.- Experience in medical industry (Preferably).**Ubicación principal**México-Chihuahua-Ciudad Juárez- **Organización**Cordis de Mexico S.A. de C.V. (8286)**Área**Ingeniería**Requisition ID**2206080521W