INGENIERO DE PROCESOS I

Johnson & Johnson MedTech; Ciudad Juárez; Presencial; USD 18,000 - 30,000; Jornada completa

Descripción de la vacante

A leading company in the healthcare sector is seeking a Process Engineer I to support project management and continuous improvement in product development. The role involves technical support, project execution, and ensuring supply chain continuity. Ideal candidates will have an engineering degree, bilingual proficiency, and relevant experience in the medical devices industry.

Formación

• 2 to 4 years of experience in product development and/or manufacturing, preferably in the medical device industry.
• Knowledge of the Quality system, GMP/ISO standards (preferably).

Responsabilidades

• Leading and executing projects to reduce process/product variation.
• Ensuring supply chain continuity through tool qualification and validation.
• Providing technical support for process changes and quality problem resolution.

Conocimientos

Bilingual in English and Spanish

Knowledge of operations, products, and processes

Proficiency in computing applications

Educación

Engineering degree

Herramientas

FEA

CAD

Statistical analysis software

Descripción del empleo

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

Job Function

Supply Chain Engineering

Job Sub Function

Process Engineering

Job Category

Scientific/Technology

All Job Posting Locations:

Ciudad Juarez, Chihuahua, Mexico

Job Description

About Cardiovascular

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

Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure, and atrial fibrillation (AFib) patients.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

We are searching for the best talent for Process Engineer I

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, to ensure an uninterrupted flow of components for assembly operations, meeting instruments, quality, cost, and delivery requirements.

You Will Be Responsible For

• Following company policies and procedures related to your work area and ensuring subordinates do the same.
• Completing required trainings within the specified timeframe, including safety and environment retraining.
• Adhering to all safety policies and promoting safety among associates.
• Leading and executing projects focused on reducing process and/or product variation to positively influence business metrics, strategic directions, and financial results.
• Maintaining updated work plans for projects including design changes, process changes, and cost improvement initiatives.
• Identifying and executing cost improvement projects to support manufacturing supply chain goals and supplier objectives.
• Directing technical projects to improve capacity, maintenance, instruments assembly, and instrument performance.
• Providing technical support for process changes, validation, and quality problem resolution.
• Potentially supervising activities in Manufacturing Engineering Science and Technology (MEST) areas.
• Ensuring supply chain continuity through tool qualification and validation.
• Closing non-conformities and ensuring timely corrections and approval of control plans.

Qualifications / Requirements

• Engineering degree
• Bilingual in English and Spanish (preferably)
• 2 to 4 years of experience in product development and/or manufacturing, preferably in the medical device industry
• Knowledge of operations, products, and processes
• Knowledge of the Quality system, GMP/ISO standards (preferably)
• Proficiency in computing, word processing, spreadsheets, presentations, database applications, and statistical analysis software
• Experience with engineering applications software (e.g., FEA, CAD) when required