Supports international registration activities including but not limited to provision of regulatory documentation such as Certificates of Free Sale. Supports legalisation activities. Facilitates the registration and notification of SJM products in EMEA .
Compiles product information and provides to regulatory affairs leaders to enable provision of regulatory submission applications to the relevant national regulatory agencies.
Liaises with the SJM EMEA QA/RA Departments and International/Product Divisions as required to answer regulatory queries and ensure that local processes meet regulatory requirements.