Regulatory Affairs - Independent Contractor

Job type:
on-site
Start:
01/2020
Duration:
6 Months
From:
Phaidon International
Place:
Frankfurt am Main
Date:
12/07/2019
Country:
flag_no Germany
project ID:
1858773


Working with a Medical Technology company to assist the teams improve their Regulatory system for a 6 month contract working flexibly from client site just outside of Frankfurt.

Senior Regulatory Associate consultant's Responsibilities:
  • Maintenance of Regulatory Files- Globally including FDA
  • Provide support for currently required products and registration with distributors
  • Collating information for what is needed for global regulatory registrations
  • License renewals
  • Compile Documents for submissions
  • Support RA team members for RA questions - knowledge transfer to the team
  • Documentation in English - German Speaking preferred


Requirements
  • Experience in Medical Device Regulatory Affairs
  • Class II / IIb Devices


There is the the possibility have home-based flexibility.