Posted:1 day ago|
Platform:
Work from Office
Full Time
2. Sound knowledge on development guidelines for EU and US for e.g. Comparative dissolution requirements ,Design of experiments ,ICH 8 ,PDR preparation as per quality by design model.
3. Coordination with purchase team for selection of suitable vendors of RM and PM for tablet and capsules.
4. Shall be responsible for Technolgy transfer of products from F&D to manufacturing site .
5. Shall be responsible for risk assessment for elemental and nitrosamine impurities along with analytical R&D.
6. To coordinate with regulatory affairs department for submission of PDRs and to answers queries from various regulatory bodies across the globe.
Ananta Medicare Limited
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