Lead the Quality System of the organisation from design technology to manufacturing process.
Lead risk management activities.
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%