- Responsible for identifying project requirements and request for indenting, monitoring receipt, consumption of Raw materials, Packing materials, consumables etc.
- Responsible for Execution of cleanliness, verification, calibration status of equipment along with resolution action plan on daily basis.
- Prepare SOPs for current equipment and procedures & Review of SOP for mandatory revision.
- Review and interpret scientific literature to guide project decisions
- Development of new formulation projects by complying GLP procedures.
- Carry out literature survey, Pharma Equivalence and Pre-formulation study during product development; Plan & perform experiments for various lab scale batches, optimization batches.
- Execution of scale up and Exhibit batches at plant level.
- Preparation & maintaining of the development batch compilation, stability batch compilation and other documentation during development.
- Preparation of PDR, MFR, Specifications, stability protocol,



stability report and relevant departmental documents.
- Carry out & execute technology transfer of finalized F&D; product along with its complete documentation to site of manufacturing.
- Any task to be fulfilled as requested by HOD in area of concern.
- Responsible for development of sterile dosage forms, in accordance with QTTP.
- Conduct experiments and analyze data to support product development by QbD concepts
- Execution & monitoring of quantitative and qualitative pre-formulation studies of sterile dosage forms.
- Develop and optimize drug formulations using appropriate technology and scientific principles

M. Pharm with 3 to 5 years experience to develop and execute the assigned projects of sterile formulations including simple & Complex (injectables & Ophthalmics).

📌 Research Associate (Kukatpally)
🏢 Aveva Drug Delivery Systems
📍 Kukatpally