Our client is a medical devices manufacturer
What's on Offer
Support and improve quality system management in compliance with applicable requirement, (ISO 9001, ISO 13485, QSR 21 CFR 820), Promote Continuous improvement process (non-conformity, CAPA and change management, Process Validation, Follow-up of production non-conformities, Participate to third parties audits (Bodies notified, authorities, ISO 13485, FDA), Manage the Continuous Improvement Plan, Promote quality system and approach in the company
The Successful Applicant
3-5 years of experience in a similar role, Level of education: Quality engineer or equivalent, or technician with significant experience in medical devices quality Knowledge of the requirements relative to the ISO13485, European directive 93/42 and 21 CFR part 820, Continuous improvement, Good skill for communication and coordination, Conscientious, Diplomat, and Rigorous, Good command of French and English.