The role involves developing parenteral formulations, conducting pre-formulation studies, and performing various stability and compatibility tests under moderate supervision.
- 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
Top Skills
Autoclave
Lyophilizer
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