Your Responsibilities: Your responsibilities include, but are not limited to:

• Work on platform device development and participate to project activities in cross-functional teams to deliver easy-to-use, safe and robust products
• Contribute to the complete development process of medical devices: ideation, brainstorming, prototyping, piloting, manufacturing and complaint handling
• Create and review IP
• Work with CAD, 3D, drawings, tolerance analysis
• Size and specify plastic and metallic components
• Work with third party suppliers, including prototyper, tool makers, CMOs
• Manage testing and characterization for acceptance, compliance, performance etc., and implement improvements
• Perform root cause analysis and develop robust solutions to prevent re-occurrence
• Ensure components are delivered and controlled to the required quality for clinical trials and commercial production
• Author key design history file documents: design input requirements, component specifications and design verification documents.