- 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.
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.