Description
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.