Development of parenteral formulations with moderate supervisionConduct pre-formulation studies and define formulation strategy.Able to perform Patent Search, Proof of concept studies for new products.Evaluate/Establish the physicochemical parameters such as Solubility profile, PKa, LogP etcFamiliar with Osmolality, Viscosity, Specific gravity, Headspace, Oxygen/light sensitivity studyShould able to perform pH stability, Freeze thaw cycling, Material compatibility studiesFamiliar with In use stability testing, Preservative effectiveness testing conceptsPerform product developability risk assessments and Drafts Scientific protocols and reports.Preparation of Stability protocols and stability sample handlingExecution of Pivotal / Process optimization batches and submission batchesApplication of Test License, Import license and NOC -review of documents.Able to understand Freeze-drying/lyophilization technique/conceptsShould be able to handle the equipment like Autoclave, Lyophilizer and manufacturing vessels.Upkeep the formulation labs for all time audit readiness.Masters in Pharmacy with 1 to 3 years of relevant experience   
Work Location Assignment: On Premise

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Research and Development