SENIOR QUALITY ENGINEER (2nd Shift)

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 jnj.com .

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.

We provide an inclusive work environment where each person is considered as an individual.

At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:
Quality

Job Sub Function:
Quality Assurance

Job Category:
Professional

All Job Posting Locations:
Ciudad Juarez, Chihuahua, Mexico

Job Description:

About MedTech

Fueled by innovation at the intersection of biology and technology, we're 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 https://www.jnj.com/medtech

We are searching for the best talent for Senior Quality Engineer to be in Salvarcar Plant, Ciudad Juarez, Chih.

Purpose: Established and productive individual contributor in a scientific/technology field.

Creates, under general supervision, Quality Engineering schematics, detailed layouts, and subsequent comprehensive supply chain outputs, as well as associated key performance metrics, goals, and objectives.

Works collaboratively with management to drive decisions regarding Quality Engineering methods to produce leading-edge customer-tailored engineering final deliverables.

Qualifications / Requirements


* Bachelor's degree in a related field


* Along with a minimum of 4 - 6 years of quality, manufacturing, or research and development experience in a medical device or other regulated industry is required.

Master's degree is preferred.


* American Society for Quality (ASQ) certification, Six Sigma experience, and/or knowledge of Process Excellence tools is desirable.


* Knowledge of GD&T (Geometric Dimensioning and Tolerancing) is desirable


* Ability to develop and implement Quality standards.


* Thorough knowledge of Quality and operations systems and processes, including GMP and QSR requirements for medical devices.


* Thorough knowledge of leading-edge Quality Engineering, design control, and verification and validation (V&V) tools and methodologies.


* Ability to apply project management skills to ensure fulfillment of new product development requirements.


* Demonstrated auditing and problem-solving skills.


* Understanding of Six Sigma and Business Excellence tools and methodologies.

Lean manufacturing experience desirable.


* Ability to tr...