Required education:

Technical Background ( Engineering , Phisics, Chemistry , Pharma)

Required experience :

6 – 10 years

Required languages:

Italian- English

Required technical skills:

ISO 13485 QMS in Medical Devices

MDD-MDR Transition knowledge Implants

Medical Device Regulation 2017/745 ,

Knowledge of Technical Documentation for Medical Devices

Clinical Evaluation Practice

ISO 14971 ISO 24971 Risk management approach and tools for medical devices

Additional experience and/or skills:

Handling Technical documentation in Medical Devices

Clinical Evaluation reporting

Post Market Clinical follow Up

Validation of Literature search of State of The Art for medical devices

Clinical Jr Specialist Medtech Implant 860