Job Title: R&D Engineer – EU Medical Device Regulation (EU MDR)Job Description
This role focuses on leading research and development activities for medical devices intended for the EU market, with a strong emphasis on compliance with the EU Medical Device Regulation (EU MDR 2017/745). You will drive design, development, documentation, and regulatory strategy to ensure products meet both technical performance requirements and global regulatory obligations. Working as part of an R&D organization, you will collaborate closely with Regulatory Affairs, Quality Assurance, Clinical, and Manufacturing teams to deliver safe, effective, and compliant medical devices throughout the product lifecycle.
Responsibilities

+ Lead and support remediation design activities for medical devices in accordance with EU MDR 2017/745 and applicable international standards.

+ Conduct engineering studies, testing, and technical evaluations to ensure that design controls fully align with re...