Beschreibung
Main tasksParticipate in the development of new products and manufacturing processes.
Coordinate the technical part and the execution of the tasks.
Develop the CAD design, technical drawings and FEA analyses.
Define and organize the verification and validation tests.
Write the documents of the technical files (DHF).
You will also be involved in risk analyses.
You will be in charge of putting new products into production internally and externally between the various stakeholders: Software Engineering, Quality Engineering, Manufacturing, etc.
Provide technical support to subcontractors and design for manufacturing.
Your profile
Bachelor degree in relevant field.
Experience in the development of medical devices.
Understanding of an essential regulated technical environment (ISO 9001, ISO 13485).
Understanding of manufacturing, machining and control techniques.
Fluent English and German.