Regulatory Affairs Associate I

1 month ago


Mumbai, India Teva Pharmaceuticals Full time

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

How you’ll spend your day

Assessment of change controls for registration impact and implementation of all necessary dossier changes in; Europe and International Market Responsible for compilation of the variations for the products in the product portfolio in collaboration with other stakeholders Compiling variation packages Experienced in managing, regulatory database and Trackwise.

Your experience and qualifications

Qualification:

Academic degree- and thinking level with a chemical/pharmaceutical background.

Experience:

2-5 years of experience in CMC Regulatory Affairs; Mainly in Europe and International Market Knowledge on registration procedures and pharmaceutical regulations Interest and capability to work with different software, including Document Management System Accurate, able to prioritize and work according to agreed timelines. Working independently with a moderate level of guidance and direction. Solve complex problems using existing solutions and support. Identify & implement process improvements. Team player

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