Vacancy expired!
Regulatory Specialist The Regulatory Affairs Specialist is responsible for coordinating activities to support of international product registrations, database management, export certificates and technical documentation.
- Maintain up-to-date knowledge of global regulations
- Support Cardinal worldwide product registrations
- Maintain country specific site registration requirements
- Maintain current regulatory databases to ensure accurate regulatory data
- Collaborate with regional regulatory teams to obtain required registration documents upon fully understanding the local regulations
- Under direction, prepare international submissions and maintain existing regulatory approvals through letter to file, renewals etc.
- Obtain regulatory information from various sources to maintain product information databases
- Organizes regulatory information resources and tracks and controls submissions.
- Organize and maintain regulatory product files
- Obtaining/Maintaining Certificates of Foreign Government (CFG)/Certificates of Free Sale (CFS)
- Bachelor Degree in scientific discipline, or significant experience in Medical Device Industry with a concentration in Regulatory Affairs
- 1-3 years Regulatory Affairs experience or equivalent required
Vacancy expired!