Job Summary
A leader in medical science is searching for a person to fill their position for a Remote Neuromod Regulatory Affairs Senior Specialist in Valencia.
Candidates will be responsible for the following:
- Preparing submissions to obtain various worldwide approvals to commercially distribute products
- Preparing required submissions to facilitate the continuation of clinical studies
- Participating in the review and submission activities
Must meet the following requirements for consideration:
- BS in Scientific discipline/engineering
- 5+ years of experience in the area of worldwide regulatory affairs in Post Marketing Assessment
- Class III Medical Device experience
- Knowledge and experience of U.S. FDA, Canada and EU regulations and standards