Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide.
Post : Regulatory Affairs Associate I
Job Description
• 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.
Candidate Profile
• Academic degree - and thinking level with a chemical / pharmaceutical background.
• 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
Additional Information
Experience : 2-5 years
Qualification : Academic degree
Location : Bangalore
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Regulatory Affairs
End Date : 20th May 2024
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