R&D Product Development Engineer

Are you passionate about innovation and transforming ideas into reality?

Do you thrive in a collaborative environment and possess a knack for problem-solving?

If so, we'd love for you to join our team as an R&D Product Development Engineer!

 Roles & Responsibilities

·   Collaborates with stakeholders and holds meetings to collect and analyze all requirements to prepare appropriate design strategies.

·   Defines end-to-end product workflow and product modes.

·   Perform FTA, responsible for SW\HW tools to make system performance analyze

·   Lead product integration activities (SW, Mech, Elect.) to validate customer requirements.

·   Conceptualize, design, prototype, test, and ship system or module features

·   Contributes to risk management file to ensure successful regulatory approval of the new product across our global markets

·   Responsible for defining System Performance requirements and ensuring design implementation and verification of performance features.

·   Develop novel system user interfaces and working procedures for product and clinic procedures

·   Conducts product human factors & usability validation activities in collaboration with RA and clinical engineering

·   Carries out field testing and bench-level testing including effectively troubleshooting analysis.

·   Writing technical documentation: specs, verification procedures, reports.

·   Lead disposable and reusable product validations as sterilization, biocompatibility, cleanability, shelf life, safety, and essential performance specifications.

·   Manage local & overseas subcontractors.

 Skills and Experience

·   B.Sc. or M.Sc. in Mechanical, or Biomedical Engineering with 3-5 years of experience in Medical devices Design Control procedures - MUST

·   Proven track record and ability to develop and test user interface products.

·   Proven track record and ability of disposable products validations.

·   Comfortable working across multiple disciplines (electrical, software, controls, human factors, clinical engineering)

·   Experience and knowledge in Quality and Regulatory aspects (ISO 14791, IEC60601, ISO 13485, CE, FDA)

·   Experience in Solidworks, LabVIEW, MATLAB, Payton & MS-Office

·   Good project management skills ( MS Teams, MS-Project )

·   Strong technical altitude.

General Requirements

·   Self-driven, Independent and well-organized

·   Fluent in Hebrew and English. Additional languages are preferred

·   Team player

Send CV to Mail: [email protected] ; [email protected]