Quality Engineer

Location: Yokneam, Haifa District, Israel

Remote Type: Hybrid Work

Time Type: Full time

Job Description

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 end-to-end quality management per product families, starting from Supplier selection and qualification, transfer to production processes and maintain supplier and process control during product lifecycle.

You will be responsible for:

• Supporting quality-related activities throughout transfer to production and production.

• Manage Process validation/ Verification activities including Suppliers guidance with Biosense process validation requirements, planning, execution, monitoring, reporting and approval

• Support change control activities through production

• Support robust key production processes (CTXs cascading, monitoring tools, PFMEA Activities reduce human error etc.)

• Nonconformance & CAPA investigations

• Leading improvement plans with suppliers

• Contributing to operations Production stabilization, trend analysis, process improvements and supplier guidance.

Qualifications and Requirements:

• BSc or Practical Engineer / BSc in Engineering / BA degree or Quality Assurance, CQE is an advantage Qualification in Quality Assurance (CQE, CQM or CQA)

• Practical knowledge of ISO13485, experience with medical device electromechanics manufacturing companies

• Demonstrated knowledge of manufacturing principles, practices and procedures

#LI-Hybrid

 

 

Required Skills:

 

 

Preferred Skills:

Business Alignment, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Data Analysis, Detail-Oriented, Goal Attainment, Human-Centered Design, Internal Controls, Issue Escalation, Problem Solving, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality Standards