• 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