Class III 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 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

Supply Chain Engineering

Job Sub Function

Quality Engineering

Job Category

Scientific/Technology

All Job Posting Locations:

Yokneam, Haifa District, Israel

Job Description

Position Summary

The Class III Quality Engineer is responsible for supporting the development of Class III medical devices in full compliance with Quality Assurance (QA) standards, regulations, and internal Johnson & Johnson procedures.

The role covers product development activities, risk management, DHF ownership, quality process implementation, audits, and cross‑functional collaboration between HTC and the BWI QA organization.

Key ResponsibilitiesProduct Development Quality (Class III Devices)

• Ensure product development activities comply with relevant standards, regulations, and internal processes.
• Lead and maintain Risk Management activities including xFMEA, risk files, and investigations.
• Review defect meetings, clinical readiness results, and escalate potential regulatory or safety issues.
• Lead design control processes and quality deliverables for Class III devices (NPD and engineering builds).
• Support and lead quality activities during transfer from R&D to manufacturing.
• Assess and approve design changes.
• Maintain and present Quality Plans, metrics, and project status.
• Lead quality investigations and escalate product‑related issues when required.
  
  

• Lead QA activities for development of tools and jigs.
• Review and approve test equipment qualification and documentation.
  
  

• Own DHF management for Class III products.
• Define and approve QA deliverables for R&D projects.
• Conduct credibility checks to ensure documentation accuracy and compliance.
• Ensure HTC development processes align with BWI Quality processes.
• Identify and implement continuous improvements in new product development processes.
  
  

• Act as QA representative for compliance with corporate J&J NPD standards.
• Perform internal product and process audits.
• Support preparation for external audits.
  
  

• Communicate business‑related issues or opportunities to management.
• Ensure compliance with all applicable regulations, policies, and procedures.
• Perform additional tasks as assigned.
  
  

• B.Sc. in Engineering (preferred).
• Advantage: Quality Assurance certifications (CQE, CSQE, CQM, CRE).
  
  

• At least 3 years of experience in QA field in medical device industry. Advantage: Experience with Quality Audits, Quality assurance in manufacturing processes and data statistical analysis. Experience in leading multi-disciplinary projects
• Advantage: Experience in statistical data analysis methodologies.
  
  

• Understanding of ISO and regulatory standards (ISO 13485, ISO 14971, MDD/MDR).
• Strong interpersonal and communication skills.
• Ability to work with remote team leadership.
• Strong English proficiency (spoken and written).
• High integrity, self‑motivation, and ability to work independently or in a team.
• Results‑driven, detail‑oriented, and organized.