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Job Location | Vishakhapatnam |
Education | Not Mentioned |
Salary | Not Disclosed |
Industry | Pharma / Biotech |
Functional Area | General / Other Software |
EmploymentType | Full-time |
Description: Handling IPQA Execution of Engg Related Filing , Reviewing the documents of ADL and QC (Analytical method validation protocol and reports, Audit trials, Routine QC sample analytical reports, Stability sample analytical reports ) Analytical method development and method transfer activity, Preparation and monitoring of stability calendar, Change control activity, Annual product review, COA preparation, Regulatory support, Statistical process control. Experience Required: 4 - 5 YearsLocation: VizagDepartment: Quality AssuranceUnit: IVSalary: At par within industry,
Keyskills :
analytical method developmentchange controlmethod transfermethod validationmethod developmentadlipqafilingtrialscontrolprotocolmonitanalyticalvalidationpreparationVariance AnalysisregulatingSeco