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Regulatory Affairs Associate I
Teva Pharmaceuticals
Full time
2+ years
Not Disclosed
Bengaluru, India
Post Date: Apr 19, 2024
End Date: Jun 19, 2024
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2+ years
Not Disclosed
Bengaluru, India
Post Date:Apr 19, 2024
End Date: Jun 19, 2024
Skills:
Regulatory Affairs
Inspection
Management
Job Description:
Responsibilities
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.
Qualification & Experience
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
Job Overview
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Salary
Not Disclosed
Role
Associate
Area of Practice
Regulatory Affairs
Experience
2+ years
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