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2.0 - 6.0 years
0 Lacs
chennai, tamil nadu
On-site
In this role, you will be responsible for preparing IP/Patent landscape and clearance reports for parenteral, ophthalmic, and solid oral products. You will also be tasked with preparing IP evaluation reports for Regulatory markets such as USA, Canada, and Latin American markets. Additionally, you will provide formulation suggestions to the developmental team and conduct FTO/infringement analysis. Your role will involve assisting in preparing infringement/non-infringement strategies for all developmental projects. Furthermore, you will evaluate all API characteristics (polymorph, particle size, purity profile, etc.) for all developmental products across various dosage forms. Qualification Req...
Posted 2 weeks ago
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