Design, develop, and/or test mechanical assemblies of implants and/or sound processors for bone conduction solutions
Collaborate with various stakeholders involved in product development (R&D, Quality Assurance & Regulatory Affairs, Operations)
Plan your own work to support the project plan
Report on progress and meeting agreed deadlines
Autonomously coordinate all design activities for a mechanical subassembly
Design and develop mechanical assemblies that meet applicable requirements
Carry out verification and characterization of mechanical subassemblies through a combination of simulations and physical lab testing
Define the requirements applicable to incoming inspection and to production and functional testing
Contribute to product sustainability (failure analysis, change management)
Document work in accordance with the company's development processes
Ensure compliance with applicable guidelines, standards, and practices
Plan and lead design reviews to validate proposed solutions
Deliver the DHF for a mechanical subassembly by collaborating with internal or external stakeholders and organize it so that it is clear and well presented.
Requirements
Engineering degree specializing in mechanics (electromechanics, micromechanics, mechatronics) with 5+ years of experience in the design of mechanical and micromechanical assemblies (CAD modeling and production), machining, injection molding, and over molding
Experience in the development of medical devices
Good knowledge of CAD software (CREO is a plus)
Knowledge of various material technologies (metal, plastic)
Experience in sterile packaging design, with knowledge of biosafety, reprocessing procedures, and sterilization qualification
Methodical, analytical, and detail-oriented, with strong critical thinking skills; recognized for being proactive in proposing solutions, both on technical issues and on improving working methods
Proficiency in English (reading, writing, speaking)