NPD Quality Engineer

This job is with Johnson & Johnson, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. 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.comJob FunctionQualityJob Sub FunctionR&D/Scientific QualityJob CategoryProfessionalAll Job Posting Locations:Yokneam, Haifa District, IsraelJob DescriptionAbout CardiovascularFueled 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/medtechWe are searching for the best talent for NPD Quality Engineer to be in Yokneam.As a NPD Quality Engineer, you will be responsible for NPI products transfer from development to production, validation activities , supporting activities related to process and production quality improvements, non-conforming products process managementThe Quality Engineer Is Mainly Responsible ForLeading NPI product transfer from development to productionManage process validation, including supplier guidance.Manage Supplier related activities ( Review and approve supplier nonconformance, Investigations and lead improvement plans with the suppliers)Manage activities related to nonconformance methodology (nonconformance follow up and reports, and product dispositions).Experience with validations (IQ/OQ/PQ/TMV) and supplier managementConduct and support NC investigations (internal and supplier non-conformances). Performing analysis of nonconforming products and presenting data in monthly meetings.Support the production team in analyzing and reporting the quality event.Responsible for Product Development processes in compliance with standards and regulations; implement methodologies and initiate improvementsLead design controls of class III devicesLead Quality activities during product developmentLeads design changes and assessmentReview Defect Meetings and Clinical Readiness Results and escalate potential RA/safety issuesQualificationsBSc in Engineering/ BA degree or Practical Engineering with Qualification in Quality Assurance (CQE).At least 5 years experience in medical systems or medical device companiesKnowledge of investigations & cause analysis.Demonstrated knowledge of manufacturing process principles, practices, and procedures.Leading multidisciplinary project and processesGood communication skills, both verbal and written in English.Good interpersonal relations, reliable and accurate, sense of urgency, and a team player.Required SkillsPreferred Skills:Agility Jumps, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Database Backup, Data Savvy, Disruptive Innovations, Issue Escalation, Problem Solving, Process Oriented, Product Improvements, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment, Report Writing