Quality Engineer

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 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:

Yokneam, Haifa District, Israel

Job Description

About Johnson & Johnson MedTech 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 a Quality Engineer role, to join our team located in Yokneam, Israel.

Purpose: The Quality Engineer is responsible for Non-conforming products process management, Analyzing trends and supporting activities related to process and production quality improvements.

You Will Be Responsible For:

• Manage activities related to nonconformance methodology (facilitate weekly meetings, nonconformance follow up and reports, product dispositions)
• Conduct and support NC investigations (internal and supplier nonconformances)
• Review and approve supplier nonconformance Investigations
• Performing analysis of nonconforming products and presenting data in monthly meetings
• Support production team in analyzing and reporting quality event

Qualifications And Requirements:

• BSc in Engineering/ BA degree or Practical Engineering with Qualification in Quality Assurance (CQE).
• Experience in medical system or medical device companies – advantage.
• Knowledge of investigations & cause analysis
• Demonstrated knowledge of manufacturing process principles, practices, and procedures
• Good communication skills, both verbal and written in English.
• Good interpersonal relations.
• Reliable and accurate.
• Sense of urgency
• Team player