At Johnson & Johnson, the largest healthcare company in the world, we come together for one purpose: to transform the history of health in humanity.
Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years.
Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.
When You Join Johnson & Johnson, Your Move Could Mean Our Next Breakthrough.
An internal pre-identified candidate for consideration has been identified.
However, all applications will be considered.
At Johnson & Johnson Medical Devices Companies, we are using our breadth, scale, and experience to reimagine the way healthcare is delivered and to help people live longer, healthier lives.
In a radically changing environment, we are making connections across science and technology to combine our own expertise in surgery, orthopedics, and interventional solutions with the big ideas of others to design and deliver doctor and patient-centric products and solutions.
We are in this for life.
We are changing the trajectory of human health, YOU CAN TOO.
Please visit https://www.jnjmedicaldevices.com/es-419 for more information.
Biosense Webster, Inc.
is recognized worldwide as a leader in the science behind the diagnosis and treatment of cardiac arrhythmias.
Guided by the needs of electrophysiologists and cardiologists, Biosense Webster has pioneered innovative technological advancements for more than 30 years.
Some might call this quite a heritage.
At Biosense Webster, we say it's just the beginning.
For more information, visit www.biosensewebster.com We are searching for the best talent for MES SPECIALIST II to be in Ciudad Juárez.
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 neededEXPERIENCE 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)