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.
Impact: Contribute to a breakthrough medical device transforming patients lives.Growth: Be part of an international and solid scale-up at a pivotal stage.
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.
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.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.
