DirecciónAt Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities, and forward progress. That’s why for more than 135 years, we have aimed to keep people well at every age and every stage of life. Today, as the world’s largest and most broadly based healthcare company, we are committed to using our reach and size for good. We strive to improve access and affordability, create healthier communities, and put a healthy mind, body, and environment within reach of everyone, everywhere. Every day, our more than 140,000 employees across the world are blending heart, science, and ingenuity to profoundly change the trajectory of health for humanity.
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 SENIOR ENGINEERING TECHNICIAN, 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:
- Provides support to Principal Technicians or Engineers in matters related to the discipline.
- Follows standardized procedures to perform his/her tasks, when applicable.
- Maintains his/her work area clean and organized.
- Initiates, adjusts, and operates basic laboratory and manufacturing equipment.
- Has completed the environmental and safety training, appropriate for his/her discipline.
- Writes technical reports in a moderate complexity manner, using graphics, and schemes to describe and illustrate operative characteristics of the system/tests, as well as dysfunctions, deviations about the specifications of designs and functional limitations.
- Solves problems related to the systems, components and electrical equipment, testing, mechanical, hydraulics or of installation.
- Performs basic operational diagnostics tests, solves problems and disconnects components, subassemblies and manufacturing systems, processes and equipment with the purpose of isolating the failures, determine a solution and perform the necessary operations. Documents all the changes.
- Ensures that the tools and testing equipment are properly calibrated and repaired, according to the
standardized operations procedures.Provides support and/or performs equipment and fixtures quotation processes for preparation for the
purchasing process. - Provides support in the installation and validation processes of equipment required in the assigned area.
- Provides support in the SPC process statistical control processes where applicable.
- Provides support and/or generates Engineering changes or ECOs.
- Correctly develops the equipment and fixture’s introduction process to clean room following procedures and requirements established, such as, for example, MAL, PM and calibrations to it.
- Enters his/her daily tasks in eCMMS or in the system assigned for that purpose.
- Responsible for communicating business related issues or opportunities to next management level.
- Responsible for ensuring 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. - 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
External Qualifications:
- Knowledge and skills to satisfactorily develop the responsibilities of the position. 6 to 8 years of experience preferably related to the position.
- High School, technical career or equivalent.
- Preferably trained in two or more of the following disciplines: electronics, mechanics, production, electro-mechanics, testing, quality and production and process statistical control, bio-medics or industrial.
- Desirable experience (current or previous) in the medical products industry.
- Desirable 60% English.
- Basic ability to read and understand technical documentation associated to the specific discipline.
- GMPs (Good Manufacturing Practices) / ISO knowledge, preferably.
- Knowledge of preventive and corrective maintenance, documentation, calibration procedures and quality systems, preferably.
- Ability to use computers and related software.
- Ability to use measuring and testing equipment associated with the specific discipline.
- Knowledge of the Campus information systems, preferably.
- Ability to successfully complete the departmental / corporate training courses in manufacturing
techniques. - Ability to use the internal documentation change system (CPDM).
