Innovative, fast-growing start-up revolutionising pediatric care with a unique Class III medical device, empowering young patients to live a better life.

Description

As Quality Engineer you are the central quality contact for the organisation.

As such you:

- Manage quality documentation for design & manufacturing process.

- Manage Risk process activities, internal and with suppliers.

- Develop and implement inspecting and testing procedures.

- Lead product batch release.

- Lead Data analysis.

- Support training activities.

- Lead Quality System according to ISO 13485.

Profile

Master degree in Mechanics, Bio-medical or equivalent.

5 years of experience in Quality Management in medical devices, ideally with Class III.

Expertise in Medical Device standards: ISO 13485, MDR 2017/745.

Good analytical skills.

Autonomous enough to evolve in a start up environment.

French and English.

Job Offer

80-100%