Quality Engineer

About the job

Are you a microtechnology engineer? Do you have good experience in the ISO 13485 environmental field? Then this position is made for you!

For our client, a Swiss company designing innovative medical devices for advanced medical applications, we are looking for a Quality Engineer at 100% for a permanent contract.

Your tasks with your new employer

• You structure and maintain the technical files of medical devices according to the current European MDR regulation
• You update the design documentation throughout the complete and technical life cycle of medical products
• You prepare regulatory compliance elements for several international markets with internal teams
• You integrate artificial intelligence tools to ensure reliability and speed up quality document management

You offer your new employer

• You are a HES or EPF engineer, or have a technical training considered equivalent in a related field
• Ideally, you have initial experience in an ISO 13485 certified environment or a regulated industry
• You are proficient in French and English, both spoken and written, with a C1 level required in both languages
• You are rigorous, analytical and curious about new digital tools applied to quality and AI

You can also benefit from the following advantages

• You hold a key role in the regulatory compliance of innovative medical devices
• Continuous training on artificial intelligence tools is offered on site
• You work daily closely with research, development and production teams
• A dynamic and caring company culture promotes mutual support on a daily basis

Have we sparked your interest? Then apply today!