At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at

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About MedTech

Fueled by innovation at the intersection of biology and technology were developing the next generation of smarter less invasive more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at Electrophysiology

Fueled by innovation at the intersection of biology and technology were developing the next generation of smarter less invasive more personalized treatments.

As Johnson & Johnson MedTech Electrophysiology we have one goal to ensure those with atrial fibrillation can live the lives they want. For more than 30 years weve been the global market leader in the science and technology of cardiac arrythmia treatment. Our suite of tools means electrophysiologists are empowered to personalize their approaches for patients with effective and reproducible workflows. Together were changing what it means to be diagnosed with atrial fibrillation or other cardiac arrhythmias.

Your unique talents will help patients on their journey to wellness. Learn more at are searching for the best talent for SENIOR ENGINEERING TECHNICIAN

Purpose: Under direct medium or null supervision documents and develops technical functions of low medium or high complexity related to tests Quality control Layout Manufacturing Modification and Assembly of the mechanical equipment and/or its components. Performs Electrical Mechanical Electro-Mechanical and testing tasks in areas such as Manufacturing Quality Engineering Tests and Development. Builds inspects calibrates (prepares requisitions to calibrate calibrations considered as setup) adjusts verifies and gives maintenance to equipment components artifacts and systems. If CSS Position: This position will have responsibilities across ETHICON and Cardiovascular and Specialty Solution (CSS) Companies Johnson and Johnson Family of Companies) including a span of multiple product platforms such as General Surgical Devices Sutures ENT Infection Prevention Electrophysiology and Surgical and Non-Surgical Aesthetics

You will be responsible for:

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 fixtures 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 following all Company guidelines related to Health Safety and Environmental practices as applicable.
• 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 / Requirements:

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).

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