functional team and marketing teams on the regulatory submission progress of specific products and ensure support appropriate action as required on regulatory submission and identify and drive ongoing improvements. Quantity and Quality: Achievements of timely submission and approvals in line with the registration business converted in line with legislative requirements. Submissions compilation and dispatch: Complete due diligence queries as they arise to ensure delivery of submissions within agreed timelines. Labelling & Artwork
support of new registrations and post-approval submissions. To ensure regulatory input is communicated to Regulatory, Regulatory Science/CMC, Supply Chain, Submissions Management, other Viatris Country Offices, Labelling Board of Health requirements are met, ensuring a submission ready dossier. Responsible that the appropriate updated on time when changes occur. Ensure a submission planning and forecasting tool is utilized to work, liaising with Regulatory Science/CMC, Submissions Management, Cluster/Markets, and other key stakeholders
Competency in medical scheme medicine claim submissions, reversals, queries. Be able to understand claim
Competency in medical scheme medicine claim submissions, reversals, queries. Be able to understand claim
commercial strategic plan with the Regulatory affairs submission plans for all markets within the region. Lead
commercial strategic plan with the Regulatory affairs submission plans for all markets within the region. Lead
identify barriers to learning Manage all training administration and ensure all compliance and audit requirements
identify barriers to learning Manage all training administration and ensure all compliance and audit requirements
Requirements: Bachelor's degree in business administration, marketing, medical and/or Sport Sciences degree
Requirements: Bachelor's degree in business administration, marketing, medical and/or Sport Sciences degree