You will contribute to 3D modeling, drafting, dimensioning, tolerance calculations...
You implement product specifications and requirements.
You drive cost efficiency through strategic material research and in-depth analysis.You Lead and support process validation activities, including IQ, OQ, and PQ, ensuring compliance with all regulatory requirements and industry standards.You manage product development risks and oversee the entire documentation cycle.
Foster strong partnerships with suppliers and contract manufacturer to support product development and industrialisation.
Bachelor's or Master's degree in Mechanical, Biomedical, Materials Science, or a related technical field.
At least 4 years of experience in product engineering development within the medical device industry, preferably with Class III products.
Proficiency in CAD : 2D and 3D.
Knowledge of the medical device industry regulations (FDA, MDR, ISO 13485 and ISO 14971).
Interested in working in agile environments, like startups.