Quality engineer

vor 3 Wochen


Chur, Schweiz Michael Page Vollzeit
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.
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.
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