MES SPECIALIST II

En Johnson & Johnson creemos que la buena salud es la base de vidas vibrantes, comunidades prósperas y progreso.
Es por eso por lo que, desde hace más de 135 años, nuestro objetivo es mantener a las personas bien en todas las edades y en todas las etapas de la vida.
Hoy, como la compañía de atención médica más grande y amplia del mundo, estamos comprometidos a usar nuestro alcance y tamaño para el bien.
Nos esforzamos por mejorar el acceso y la asequibilidad, crear comunidades más saludables y poner una mente, un cuerpo y un medio ambiente saludables al alcance de todos, en todas partes.
Todos los días, nuestros más de empleados en todo el mundo combinan corazón, ciencia e ingenio para cambiar profundamente la trayectoria de la salud para la humanidad.
La Diversidad, Equidad e Inclusión son esenciales para continuar construyendo nuestra historia de pioneros e innovación, que ha estado impactando la salud de más de mil millones de pacientes y consumidores todos los días durante más de 130 años.
Independientemente de su raza, creencia, orientación sexual, religión o cualquier otro rasgo, TÚ eres bienvenid(o/a) en todos los puestos vacantes en la compañía de cuidado de la salud más grande del mundo.
Cuando te unes a Johnson & Johnson, tu movimiento podría significar nuestro próximo avance.
Biosense Webster, Inc.
es el líder mundial en la ciencia del diagnóstico y tratamiento de trastornos del ritmo cardíaco.
La compañía se asocia con médicos para desarrollar tecnologías innovadoras que mejoren la calidad de la atención para pacientes con arritmia en todo el mundo.
Biosense Webster es parte de la familia de empresas Johnson & Johnson.
Puedes encontrar más información en www.
iosensewebster.
om We are searching for the best talent for MES SPECIALIST II to be in CIUDAD JUAREZ.
JOB SUMMARY Under minimal and/or limited supervision, he/she works on assignments complex by nature, in which considerable judgement, judgement, and initiative are required to solve problems and make recommendations.
Provides guidance, training, and direction to less experienced employees.
Performs non-standardized or uncommon tasks related to information system configuration, validation, maintenance, change management and installation of computer manufacturing systems and applications and their components; performs installation of systems; generates and executes tests in areas of Manufacturing, Quality, and Engineering.
Develops, builds, inspects, calibrates, adjusts, verifies, improves, and maintains components related to the MES system.
Performs tasks related to computerized system interfaces and databases.
Attends non-conforming Quality actions, CAPA actions or audit requirements.
The activity of this position also includes the improvement and updating of manufacturing procedures, and Compliance activities.
Compliance with Good Manufacturing Practices (GMP's) by raising observations and communicating them to their supervisor for correction).
DUTIES & RESPONSIBILITIES Under general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position.
Representee of MES team to change request owner Supports shopfloor control team based on business impact Performs change intake process and understands requirements Performs change/impact assessments for MESDC Maintains and improves MES SOP’s Maps new processes or processes undergoing change Writes ECO’s, documents NR’s OBS, AP Takes voice of the customer and proposes internally how to improve processes Performs training and supports new hire introduction Participates in the administration and configuration of MES and connected systems.
Coordinate and deliver training to MES users.
Provides support in the development, testing, validation, and implementation of configurations of such systems.
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.
Provides sustaining support to the MES and connected systems 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 QA non-conformities and Observations.
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 communicating business related issues or opportunities to next management level For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures Performs other duties assigned as needed Qualifications EXPERIENCE AND EDUCATION Studies in Technical Career or equivalent applicable to the area.
Mechanical; Electrical; Electromechanical; Electronic; Information Technology; Industrial or system preferably.
Knowledge and Skills to successfully develop the responsibilities of the position.
Experience in conducting system integration test, user acceptance test and production rollout preferably Experience in user problem understanding, requirements gathering, analysis, design and solution proposal preferably REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS* Extensive knowledge in computational packages.
Excellent verbal and written communication skills including the ability to write technical documentation and communicate technical information to non-technical audiences.
Ability to read and understand technical documentation associated with the specific discipline.
Advanced Language level.
Spanish/English.
Knowledge of GMP's (Good Manufacturing Practices) / ISO (Preferably) Knowledge in process and SDLC validation activities (Preferably) Knowledge of FDA regulations 21-CFR part 820 and Part 11 (Preferably).
Knowledge of SQL DB (Preferably) Knowledge of programming tools (Python, Microsoft Apps, etc.) (Preferably) Knowledge in CAMSTAR (Preferably).
Knowledge of JDE, CMMS, cPDM, Windchill, SAP (Preferably) Knowledge in Engineering Changes ECOs.
(Preferably) Experience in medical industry (Preferably)