- Responsible for identifying project requirements and request for indenting, monitoring receipt, consumption of Raw materials, Packing materials, consumables etc.
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Responsible for Execution of cleanliness, verification, calibration status of equipment along with resolution action plan on daily basis.
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Prepare SOPs for new equipment and procedures & Review of SOP for mandatory revision.
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Review and interpret scientific literature to guide project decisions
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Development of new formulation projects by complying GLP procedures.
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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.
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Preparation & maintaining of the development batch compilation, stability batch compilation and other documentation during development.
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Preparation of PDR, MFR, Specifications, stability protocol, stability report and relevant departmental documents.
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Carry out & execute technology transfer of finalized F&D product along with its complete documentation to site of manufacturing.
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Any task to be fulfilled as requested by HOD in area of concern.
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Responsible for development of sterile dosage forms, in accordance with QTTP.
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Conduct experiments and analyze data to support product development by QbD concepts
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Execution & monitoring of quantitative and qualitative pre-formulation studies of sterile dosage forms.
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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).
