Your Responsibilities
- Participate in the design and development of new medical devices and improve existing product lines
- Ensure project timelines and compliance with regulatory requirements (ISO 13485, 21 CFR Part 820, MDR 2017 / 745)
- Collaborate with cross-functional teams (marketing, industrialization, regulatory affairs, and quality) at all project stages
- Design products and create technical drawings (SolidWorks) while ensuring compliance with functional and regulatory requirements
- Manage technical documentation (DHF, test reports, design specifications)
- Contribute to the industrialization of new products
Your Profile
Mechanical engineering degree (or equivalent) with at least 7 years of experience in the design and manufacturing of technical productsExpertise in GD&T and proficiency in SolidWorksExperience in a medical device industry is mandatoryAbility to propose innovative and efficient technical solutionsStrong team spirit, rigor, and autonomyFluent English and French (written and spoken)Knowledge of orthopedic devices is a plusWhat We Offer
A dynamic and international work environmentA young and motivated teamModern office space with excellent facilitiesSports activities during lunch breaksRemote work : 1 day per weekAttractive social benefits packageAre you passionate about innovation and looking to join a key player in the medical devices field ? Apply quickly now!
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