Job Description
You will be responsible for managing the global submission process for assigned products of Merck’s General Medicines portfolio.
The Marketed Product Lead Thyroids is responsible for the regulatory strategy for Euthyrox, Thyrozol, Novothyral, Jodthyrox and Jodid with the new formulation of Euthyrox as the main project for the upcoming years in over 100 countries worldwide, but also new marketing authorisations in the frame of up to double digit growth in sales. This will include the creation and review of regulatory documents and documentation, the management of submissions to countries of the ICH regions with a main focus on Europe, Canada, Israel and Australia and the support of submission activities in non-ICH regions in cooperation with an external vendor. You will be member of a Regulatory Subteam and Clinical Trial Teams for assigned products and will closely cooperate with various headquarter functions and with country regulatory units of the Merck organization.