Provide technical leadership in system integration, testing, verification, problem-solving and product improvements.
Oversee and be deeply acquainted with development processes regulated by relevant standards Risks, usability etc. Ensuring systems design and documentation comply.
Hands-on work on system HW components and SW when developing new capabilities and features.
Attend R D labs and surgeries observation for in-depth clinical knowledge.
Work closely with relevant stakeholders: PMO, Product, Clinical, Service, QA, DA etc..
Support key processes in the development life cycle, such as: sustainability investigations, SW and HW optimization, technical experiments, Risk management, usability validation and UI / UX specifications.
Requirements: B.Sc or M.Sc from a known institute in the fields of electrical/robotics/ system engineering.
Experience through the full product development cycle of complex medical device systems, or other regulated fields, from initial concept to release to market.
Demonstrated technical leadership and ownership.
Proven ability for analytical problem solving, troubleshooting and issues investigations.
Ability to provide guidance and direction to less experienced technical personnel.
Track record of strong cross-functional collaboration, influence, and management capabilities enabling highly effective project teams.
2+ years of work experience as a system Eng. in medical devices or other highly regulated industries.
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