TECNICO DE INGENIERIA PRINCIPAL (SEGUNDO TURNO)

At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through 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 humanity.
Learn more at https://www.
nj.
om/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.
We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
We are searching for the best talent for ENGINEERING TECHNICIAN PRINCIPAL to be in Cd.
Juarez, in plant Horizontes.
JOB SUMMARY 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.
DUTIES & RESPONSIBILITIES Under supervision 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 EXPERIENCE AND EDUCATION Knowledge and skills to satisfactorily develop the responsibilities of the position.
8 to 10 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-medical or industrial.
Experience (current or previous) in the medical products industry.
Desirable 70% English.
REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS 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).