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Ingénieur Qualité R&d (dispositifs Médicaux) F/h/x
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NEMERA
Lyon, France
Onsite
Design control
Risk management
Regulatory compliance
Skills & Requirements
Must-have
Design Control
Risk Management
Regulatory Compliance
Documentation
Project Coordination
Testing Procedures
Material Compliance
Nice-to-have
Team Collaboration
Problem-Solving Skills
Cross-Functional Communication
Language Proficiency (English)
Key Requirements
5 years of experience in medical device development
Knowledge of ISO 13485:2016, ISO 14971:2019, MDR 2017/745, 21CFR820
Experience with plastic injection processes
Fluent in English
Work Rights
Not specified
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