Cdd - Responsable Evaluation Clinique De Dispositifs Médicaux Logiciels (f/h)

GE HealthCare Technologies

Buc, France
Not specified; not specified; not specified
Hybrid
Medical device regulatory compliance
Clinical evaluation report writing
Post-market surveillance coordination
GE HealthCare Technologies is seeking a Clinical Evaluation Leader for a hybrid role in Buc, France. The candidate will be responsible for defining and executing clinical evaluation strategies for medical software products, ensuring compliance with regulatory standards and delivering projects on time and within budget

Job Summary

  • The role involves defining and executing the clinical evaluation strategy for software-based medical devices to ensure market delivery and maintenance.
  • Candidates will coordinate with project teams and clinical stakeholders to manage post-market surveillance data and update clinical evaluation reports.
  • This position requires leading the transition to European regulations and ensuring all existing product reports meet current safety and performance standards.

Matching Summary

Match Score: 85

GE HealthCare Technologies is seeking a Clinical Evaluation Leader for a hybrid role in Buc, France. The candidate will be responsible for defining and executing clinical evaluation strategies for medical software products, ensuring compliance with regulatory standards and delivering projects on time and within budget.

Salary

Not specified; Not specified; Not specified

Skills & Requirements

Must-have

  • Medical device regulatory compliance
  • Clinical evaluation report writing
  • Post-market surveillance coordination
  • Software as a medical device expertise
  • French and English fluency

Nice-to-have

  • Experience in medical imaging
  • Strong cross-functional collaboration
  • Autonomous problem solving
  • Continuous improvement mindset
  • Audit representation experience

Key Requirements

  • Engineering degree or Master's level (Bac+5) required
  • Experience in medical imaging and pathology
  • Fluent in French and English
  • Knowledge of medical device regulations and quality systems

Work Rights

Not specified

Tailored Resume

Cover Letter