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| Job Location | Ahmedabad |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Manufacturing |
| Functional Area | Bio Tech / R&D / Scientist |
| EmploymentType | Full-time |
*Execution of NCE projects, generic projects and line extension projects using QbD principle.Preparation and/or review of literature summary and development report to the assigned product.Involve in execution and/or supervision of formulation development, process development and manufacturing of GMP batches to the assigned product.Preparation and/or review of technical documents like MFC, BMR, BPR and Stability protocol etc. following the GDP.Execution and/or supervision of scale up and pilot batches in pilot under GMP condition.Preparation and/or review of technology transfer documents and transfer of technology to manufacturing site, if required.Performing and/or supervision calibration and maintenance of R&D instruments and equipmentProcuring/ indenting materials and machines change parts related to concern projectsMaintain safe and hygienic condition in respective departmentEnsuring the use of personal protective equipment whenever required during batch executionAttending training related to FD, EHS and QA (if applicable)All generated waste to be sent to concerned person and must be comply with EHS requirementsCommunicating and interacting with international and national clientsPreparing and/or reviewing of proposals for upcoming new projects, *M.Pharm in Pharmaceutics/Ph.D
Keyskills :
researchhplctechnology transfervalidationapicontinuous improvement facilitationnew projectsmusic makingprocess developmentformulation developmentstability protocolscale upehs