A fast-growing medical device company focused on developing, manufacturing, and selling innovative devices for endovascular interventional procedures. We are looking for a talented and creative engineer to join our R&D team and be a key player in our future development.
LOCATION: Yokneam, Israel
SCOPE & RESPONSIBILITIES:
Design and develop innovative neurointerventional medical devices as part of the R&D team.
* Plan and execute verification tests for new prototypes and new products
* Prepare product documentation, including DHF and DMR
* Analyze TEST results and author detailed engineering reports
* Collaborate with Quality and Regulatory Affairs to ensure design control compliance
* Lead design transfer activities, support pilot production, and transition products into manufacturing
LOCATION: Yokneam, Israel
SCOPE & RESPONSIBILITIES:
Design and develop innovative neurointerventional medical devices as part of the R&D team.
* Plan and execute verification tests for new prototypes and new products
* Prepare product documentation, including DHF and DMR
* Analyze TEST results and author detailed engineering reports
* Collaborate with Quality and Regulatory Affairs to ensure design control compliance
* Lead design transfer activities, support pilot production, and transition products into manufacturing
Requirements:
* Bachelors degree in Mechanical or Biomedical Engineering from a leading university, GPA 85+
* 2-5 years of experience in a relevant engineering role
* Hands-on experience in the medical device industry – an advantage
* Familiarity with design control processes and standards (ISO 13485, FDA 21 CFR 820) – an advantage/
* Proficiency with SolidWorks – an advantage
* Full proficiency in English, including reading and writing technical documentation
* Team player with strong communication skills, self-driven and detail-oriented
* Bachelors degree in Mechanical or Biomedical Engineering from a leading university, GPA 85+
* 2-5 years of experience in a relevant engineering role
* Hands-on experience in the medical device industry – an advantage
* Familiarity with design control processes and standards (ISO 13485, FDA 21 CFR 820) – an advantage/
* Proficiency with SolidWorks – an advantage
* Full proficiency in English, including reading and writing technical documentation
* Team player with strong communication skills, self-driven and detail-oriented
This position is open to all candidates.
