Research Associate

• 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 new 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

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