Back to jobsAssist in the development of devices through prototyping, testing, and 3D modeling.
Create and conduct verification and validation testing to validate design requirements and concepts.
Prepare regulatory filings to various government bodies alongside our IP and Regulatory Affairs teams.
Support clinical trials of devices and work with external suppliers and clinicians.
Aid in the development and provision of technical documentation by preparing drawings, writing work instructions, and presenting technical insights.
Monitor safety practices and ensure ISO 13485 and FDA compliance while collaborating with cross functional teams to meet product timelines.
In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.
Other duties as required.
