Job 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 products
Expertise in GD&T and proficiency in SolidWorks
Experience in a medical device industry is mandatory
Ability to propose innovative and efficient technical solutions
Strong team spirit, rigor, and autonomy
Fluent English and French (written and spoken)
Knowledge of orthopedic devices is a plus
What We Offer
A dynamic and international work environment
A young and motivated team
Modern office space with excellent facilities
Remote work: 1 day per week
Attractive social benefits package
Are you passionate about innovation and looking to join a key player in the medical devices field? Apply quickly now!
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