QUALITY ENGINEER I

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.jnj.com/.

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.

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When You Join Johnson & Johnson, Your Move Could Mean Our Next Breakthrough.

We are searching for the best talent for Quality Engineer I to be in Juarez, Chih.

Salvarcar Plant

Purpose:

Adds value through the knowledge of process engineering; provides support to the stabilization and to the life cycle of projects for continuous improvement from the identification to the execution and closing in terms of cost, quality, efficiency and time cycle.

Quick response to operations in: technical resolutions, change of direction, manufacturing scalability, process development/operations product and material replacement.

Can complete projects in his/her work area or with suppliers, in order to provide an interrupted flow of components for the assembly operations, that has the established requirements of instruments, quality, cost and delivery times .

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:


* Primary responsibilities include assisting in a supporting role on new product development, sustaining and supply chain quality projects.

Assist in the development of effective quality control and associated risk management plans.


* Write process and product validation protocols and reports, equipment qualifications, engineering change orders.


* Use statistical tools to analyze data, make acceptance decisions, and improve process capability (Six Sigma, SPC, DOE).


* Help to ensure that development activities follow design control requirements, product is tested per applicable standards, European Essential Requirements are met per the MDR, and product is properly transferred to manufacturing.


* Provide support in quality improvement opportunities as appropriate to legacy products, continuous improvement and customer satisfaction


* Assistin planning necessary to ensure effective product acceptance.

This includes, but is not limited to, inspection instructions, equ...