Review of Literature summary report, patent summary report and development protocols. o New product development, Planning and Resource allocation for Domestic and ROW Market. o Alternate source development for API and Excipients, GC improvement of existing products. o Timely execution of scale up/ exhibit/process validation of allotted projects. o Process improvement and troubleshooting of existing commercial products. o Overall review of Formulation Development data during stage gate clearance. o Execution of allotted projects in stipulated timeline & within budget. o To check feasibility of manufacturing and costing of all new projects for UID. o Timely review of LNB and project files for allotted projects. o To coordinate with CFT team like AR Lab, Production, Manufacturing, QA/QC for timely completion of project. o Ensure timely address of regulatory deficiencies for Domestic and ROW Market. o Compilation and review of the FnD data, interpretation and summarize the recommendations. o Preparation and Review of technical documents such as MFC, SOP, PDR, TTD protocol, MMD, FPS and development protocol. o Ensuring the availability of manufacturing and analytical requirements/documents and resources before execution of batches at plant. o To evaluate the deviations noticed during technology transfer at shop floor and perform root cause analysis and rectification after consultation with the concerned department. o Ensure adherence to guideline in various product development activities during development
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