Medical Device Regulatory Affairs International Registrations
Regulatory Affairs International Registrations
Our client is currently in the process of getting approvals for exporting their medical devices. They need regulatory affairs specialists who have help companies go through the process of exporting medical devices. The experience the client is looking for includes, but is not limited to, international registrations, licensing, interfacing with foreign governing bodies, etc.
Day to Day Responsibilities:
This consultant will be responsible conducting hands on work for the Director of Regulatory Affairs. This individual will be submitting international registrations and helping the client receive approval to export products to numerous locations. In addition to registering the project, this regulatory affairs specialist must have experience working with licensing, labeling, and any other aspect involved in getting a medical device approved for exporting.
Medical Device Exportation approvals
Job Type: Contract