QA Operation Platform lead

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

Quality Engineering

Job Category

Scientific/Technology

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 QA Operation Platform Lead role, to join our team located in Yokneam, Israel.

Purpose: As a QA Operation Platform Lead, you will be responsible for end-to-end quality management per product families, starting from supplier selection and qualification, and maintaining supplier and process control during product lifecycle.

You Will Be Responsible For

• Supporting quality-related activities throughout production.
• Reviewing and approving supplier non-conformances, Investigations and leading improvement plans with suppliers
• Contributing to operations Production stabilization, trend analysis, process improvements and supplier guidance.
  
  

• BSc or Qualification in Quality Assurance (CQE, CQM or CQA)
• Practical knowledge of ISO13485, Experience in the Medical Device industry or medical field
• Demonstrated knowledge of manufacturing principles, practices and procedures
• Ability to lead multidisciplinary projects and processes
• Good communication skills, both verbal and written in English.
• Strong interpersonal relations
• Analytical and problem-solving skills and ability to learn
• Sense of urgency
• Ability to communicate effectively with a diverse clientele base and work cooperatively with coworkers