Our client, a leading multination in Longford, is seeking a Regulatory Affairs Specialist on a 12 month contract.
Provide support to Reg Affairs related issues.
Provide update and maintain status of product registrations and notifications.
Provide documentation and certification
Review changes for Regulatory impact.
Third level qualification in biomedical areas.
2-3 Quality/Manufacturing background within pharmaceutical or medical devices.
For a confidential discussion and more information on the role, please contact Colin Byrne.