Posted:1 day ago|
Platform:
Work from Office
Full Time
Role & responsibilities 1. To develop Stable and Bioequivalent solid oral products for US, Europe, ROW and Domestic Markets. 2. Technology transfer of developed products to plant level, this includes all TTD-related works. 3. To collect and compile all data and submit to respective regulatory agencies. 4. To address DCGI/ regulatory agency queries as per requirement. 5. To extend support to plant for any commercial trouble shooting. Preferred candidate profile Only for Phd Candidates
Cadila Pharmaceuticals
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