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Diversity, Equity & 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.

Biosense Webster, Inc. is the global leader in the science of diagnosing and treating heart rhythm disorders. The company partners with clinicians to develop innovative technologies that improve the quality of care for arrhythmia patients worldwide. Biosense Webster is part of the Johnson & Johnson Family of Companies. More information can be found at www.biosensewebster.com

We are searching for the best talent for ENGINEERING TECHNICIAN (TEMPORARY 12 MONTHS), to be in Ciudad Juarez, Mx.

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).

You will be responsible for:

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

Qualifications and requirements:

• 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.
• 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)