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Design Assurance Engineer

  • Israel
  • Quality Assurance and Regulation
  • Full-time
  • On-site
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Description

We're looking for a Design Quality Assurance Engineer to join our growing Design QA team.

In this role, you’ll collaborate closely with R&D, Engineering, and Manufacturing teams to support the design and development process and regulatory compliance.

As we continuously evolve our product and processes toward PMA (Pre-Market Approval), this is a unique opportunity to join at a high-impact phase of development.

Responsibilities

  • Ensure that design and development activities are performed in accordance with applicable procedures and approved design and development plans.
  • Work closely with project teams to provide quality and compliance input throughout the design and development process.
  • Review and approve key design and development deliverables, including requirements, design outputs, and verification and validation documentation.
  • Support Regulatory Affairs activities, including regulatory submissions, responses to regulatory questions, implementation of new or revised standards, and internal and external audits.
  • Participate in project and design review meetings.
  • Perform Design Quality activities within the product risk management process, including review and approval of DFMEA and related risk management documentation.
  • Support and accompany Engineering Change Orders (ECOs), including assessment and completion of applicable quality activities.
  • Provide Design Quality support for design transfer of new products and sustaining changes to Manufacturing, Operations Quality, and Supplier Quality.

Reports to

QA Manager

Requirements

  • At least 3-5 years of experience working in a quality function in the medical device industry – must.
  • At least 2-3 years of experience as a design control engineer (preferred).
  • Prior hands-on experience in Verification & Validation (V&V) activities within the medical device industry – a significant advantage.
  • A Bachelor of Science in Engineering, Sciences, or a related field – must.
  • Experience with ISO 13485, ISO 14971, 21 CFR 820, EU MDR standards – must.
  • Familiar with statistical techniques used in verification and validation processes (preferred).
  • Strong analytical and problem-solving skills, with keen attention to detail.
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively across functions.
  • Strong execution and follow-up skills
  • Ability to work in a fast-paced environment
  • Proficient use of standard MS Office applications.
  • Fluent in English (oral and written).


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