The company is a fast-growing international scale-up in the medical device sector, dedicated to developing and industrializing life changing solution.
With a mission-driven culture and a highly motivated interdisciplinary team, it offers a dynamic environment where innovation, quality, and impact are at the heart of everything they do.
* Drive design transfer from R&D to production.
* Define and optimise manufacturing processes for pilot and commercial phases.
* Manage scale-up activities and coordinate suppliers and partners.
* Oversee process validation and ensure traceability.
* Ensure compliance with ISO 13485, MDR, and FDA regulations.
* Collaborate with Quality to maintain standards and continuous improvement.
* Monitor production KPIs and manage day-to-day operations.
Contribute to the industrialisation of a breakthrough medical technology.
Join at a pivotal stage with real ownership and visibility.
Work with a motivated, international and interdisciplinary team.
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* Engineering degree (Industrial, Biomedical, Mechanical, or similar).
* 5+ years in medical device production or industrialisation.
* Knowledge of applicable medical device regulations.
* Proven track record in design transfer and product industrialisation.
* Hands-on, proactive, and comfortable in a fast-paced environment.
* Fluent in English; French is a strong plus.
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Michael Page recrute pour les entreprises des cadres confirmés, en CDD et CDI, grâce à l'expertise de 150 consultants répartis au sein de 17 divisions.