Job Description

Development of parenteral formulations with moderate supervision Conduct 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 etc Familiar with Osmolality, Viscosity, Specific gravity, Headspace, Oxygen/light sensitivity study Should able to perform pH stability, Freeze thaw cycling, Material compatibility studies Familiar with In use stability testing, Preservative effectiveness testing concepts Perform product developability risk assessments and Drafts Scientific protocols and reports. Preparation of Stability protocols and stability sample handling Execution of Pivotal / Process optimization batches and submission batches Application of Test License, Import license and NOC -review of documents. Able to understand Freeze-drying/lyophilization technique/concepts Should 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

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Research and Development