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| Job Location | Gandhidham |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | harma / Biotech |
| Functional Area | Quality (QA-QC) |
| EmploymentType | Full-time |
Analysis and reviewing of documents like RM, FP, PM, Calibration report, validation report.Cross verification of inward register of raw material and retest raw material register and drug product.Checking of Calibration documents and maintenance of instruments as per allotment.Verification of control sample registers of Raw material.Coordinate with QA personal for revised technical documents as well as GTPs.Overall responsibility of Working Standards and procurement of Reference StandardsOperation and maintenance of Gas Chromatography and HPLC with column inward and usage record.Generation of requirement regarding chemicals, reagent, reference standard and other Q.C related items.Analyst certification of new chemists.To maintain the training schedule and related records.Maintaining all log book of instruments as well as generalTo maintain the training schedule and related recordsPlanning for the Analysis of vendor samples as well as routine analysis and report to concern and maintain the records in time.OOS investigation
Keyskills :
pharmaceuticalsmhravalidationwhodocumentationusdfaooshplceviationanalyticalmethoddevelopmentuplcchangecontrolstabilitystudiesoosanvisaqmsqualityauditqualitycontrol