NPD Quality Engineer

Posted 15 Days Ago
Be an Early Applicant
Yokneam
In-Office
Mid level
Healthtech • Pharmaceutical • Manufacturing
The Role
The NPD Quality Engineer will ensure compliance with medical device regulations, lead quality activities for product design transfers, and validate computerized systems.
Summary Generated by Built In

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:

Yokneam, Haifa District, Israel

Job Description:

About 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 NPD Quality Engineer to be in Yokneam.

We are seeking a Quality Engineer with 3–5 years of experience to join our Class III Quality team. This unique role combines two core functions:

Design Transfer QA – Lead and coordinate quality activities during the transfer of Class III medical devices from R&D to production.

Computerized Systems Validation (CSV) – Plan and execute validation activities for non-product GxP computerized systems (e.g., Polarion, eDHR, Windchill, and software tools used for product testing).

This position requires ownership, proactive problem-solving, and collaboration with cross-functional teams in a regulated medical device environment.

Key Responsibilities

  • Ensure compliance with ISO 13485, ISO 14971, FDA, and EU regulations during product development and design transfer.
  • Lead risk management activities (e.g., FMEA) and quality investigations.
  • Coordinate quality activities for new product introduction and design changes.
  • Develop and approve validation plans and protocols for GxP systems and testing tools.
  • Execute validation activities in compliance with SDLC, FDA 21 CFR Part 11, and EU Annex 11.
  • Collaborate with R&D, Manufacturing, Regulatory Affairs, IT, and Supply Chain to ensure smooth design transfer and validation processes.
  • Support internal audits and preparation for external audits.
  • Drive continuous improvement initiatives in QA and CSV processes.

Qualifications

  • Education:

    • BSc in Engineering, Quality Assurance, Computer Science, or related field (preferred).
    • Quality certifications (CQE, CSQE, CQM, CRE) – an advantage.
  • Experience:

    • 3–5 years as a Quality Engineer and/or CSV specialist in a regulated environment (medical devices preferred).
    • Hands-on experience with design transfer and risk management.
    • Practical experience in validation of GxP systems and software tools.
  • Skills:

    • Strong knowledge of ISO 13485, ISO 14971, FDA 21 CFR Part 11, EU Annex 11.
    • Excellent communication and interpersonal skills.
    • Ability to work independently and lead small projects.
    • Proficiency in English (written and spoken).
    • Detail-oriented with strategic thinking and problem-solving abilities.

Additional Information

  • Reports to: Class III QA Team Leader
  • Interfaces with global teams in the US and Europe.
  • Willingness to collaborate across time zones.

#LI-Hyberid #LI-LM5



Required Skills:



Preferred Skills:

Top Skills

Edhr
Eu Annex 11
Fda 21 Cfr Part 11
Iso 13485
Iso 14971
Polarion
Windchill
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The Company
HQ: New Brunswick, NJ
143,612 Employees
Year Founded: 1886

What We Do

Profound Change Requires Boldness.

Johnson & Johnson is the largest and most broadly based healthcare company in the world. We’re producing life-changing breakthroughs every day, and have been for the last 130 years.

The combination of new technologies and your expertise enables amazing things to happen. Teams from J&J’s consumer business are creating digital tools to help people track the health of their skin. Those working in medical devices are 3-D printing artificial joints personalized for each patient, while researchers in pharmaceuticals use AI to discover lifesaving drugs. Imagine what the rest of our team of 134,000 people at 260 companies in more than 60 countries across the world is accomplishing. We redefine what it means to be a big company in today’s world.

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