Supplier 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 https://www.jnj.com

Job Function:
Quality

Job Sub Function:
Supplier Quality

Job Category:
Professional

All Job Posting Locations:
IL001 Yokneam

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 Supplier Quality Engineer role, to join our team located in Yokneam, Israel.

Purpose: As a Supplier Quality Engineer, you will manage end-to-end quality for product families, including supplier selection and qualification, monitoring and improving supplier’s performance, support to align supplier management processes with corporate and MD.

You will be responsible for:


* Leading and managing supplier Selection, Qualification, and approval processes


* Monitoring and improving supplier’s performance


* Managing the Approved supplier list activities


* Support quality-related activities throughout production.


* Review and approve supplier non-conformances and investigation


* Leading improvement plans with suppliers.


* Contribute to production stabilization, trend analysis, process improvements, and guide suppliers.

Qualifications and Requirements:


* BSc or Certification in Quality Assurance (CQE, CQM, or CQA).


* Experience in a multidisciplinary company – mandatory.


* Practical knowledge of ISO 13485 – an advantage.


* Experience with medical device electro-mechanics manufacturing companies – an advantage.


* Demonstrated knowledge of manufacturing principles, practices, and procedures.


* Experience with evaluation, qualification and auditing suppliers – an advantage.

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