Strefa Klienta
Our client is a medical devices manufacturer
What's on Offer
Permanent contract
Job Description
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.
Powiadomienie - oferty pracy
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