Senior 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:

Caesarea, Haifa District, Israel

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 Supplier Quality Engineer to be in Caesarea

About The Role

We are looking for a Senior Supplier Quality Engineer to lead and support supplier quality activities, ensuring compliance with global standards and driving continuous improvement across our supply chain. This role is critical for maintaining robust supplier management programs and mitigating risks in manufacturing and development processes.

Key Responsibilities

• Coordinate supplier quality activities through collaboration with procurement, QA, engineering, and suppliers.
• Support and sustain supplier management programs for manufacturing and development.
• Manage service level agreements, performance metrics, and ensure contractual obligations are met.
• Address supplier quality and performance issues; identify and certify alternative suppliers to reduce risk.
• Track and trend supplier performance, provide reports to management, and implement corrective actions.
• Perform supplier audits, manage SCARs, and drive root cause investigations and corrective action plans.
• Analyze performance data to identify improvement opportunities.
• Ensure compliance with health, safety, environmental, and regulatory requirements.
  
  

• Scientific academic background (B.Sc. in Engineering preferred).
• Minimum 5 years’ experience in Medical Device Supplier Quality.
• Strong understanding of cGMP, FDA 820 QSR, ISO 13485, ISO 9001.
• Experience in statistics (DOE, MSA, Gage R&R), Six Sigma, Lean.
• Advantage: CQE certification and/or Certified Auditor.
• Excellent English (written and verbal).