Ingénieur Qualité R&d (dispositifs Médicaux) F/h/x

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

Tailored Resume

Cover Letter