Medical Device Company | Caesarea | Hybrid (4 days onsite, 1 day remote)
A medical device company located in Caesarea is seeking a Design Quality Engineer to join its R&D organization for a 9-month full-time engagement, supporting the development of an innovative Class III implant.
Key Responsibilities:
- Lead hands-on Design Quality activities throughout the full product development lifecycle
- Own and maintain Design Control deliverables
- Actively manage and maintain the Design History File (DHF)
- Lead Risk Management activities, including Hazard Analysis and Design FMEA
- Support planning and execution of Verification & Validation (V&V) activities
- Collaborate cross-functionally to ensure traceability and alignment between User Needs, Design Inputs, Design Outputs, and implemented risk controls
- Participate in design reviews, design transfer activities, change impact assessments, and regulatory submission readiness
Requirements:
- B.Sc. in Engineering or related discipline
- Proven experience in Design Control within the medical device industry
- Hands-on experience managing DHF documentation
- Experience with Class III medical devices – strong advantage
- Ability to work effectively within cross-functional R&D teams
- High level of English proficiency (written and spoken)