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.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.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.