We are looking for a Technical Writer to join our team.

Group 10
Responsibilities

As a Technical Writer, you will support the team of Design Quality of our customer to draft Risk Management documents, procedures on design control and V&V.

Group 12
Profile

The expected skills for this position are as follows:

  • Technical Background ( Engineering, Physics, Chemistry, Pharma)
  • 1-3 years of experience
  • Proficiency in English and Italian
  • ISO 13485 QMS in Medical Devices, specifically for chapt 7.3
  • Design Control
  • Medical Device Regulation 2017/745
  • Knowledge of Technical Documentation for Medical Devices
  • ISO 14971 and ISO/TR 24971 Risk management approach and tools for medical devices

024 - Technical Writer

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