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| Job Location | Ahmedabad |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Management Consulting / Strategy |
| Functional Area | ProductionSales / BD |
| EmploymentType | Full-time |
Responsible for preparation , issuance & review of BPR & BMR.Responsible for In - process checks during manufacturing in Tablet (Granulation , Compression , Coating & Packing) & Liquid Oral (Liquid Oral Manufacturing & Liquid Packing Line) , to give theline clearance for start of activity in production & stores area.Preparation , execution and review of various qualification protocols and ensuring completion ofprotocol and report.Preparation , review , distribution of Standard Operating Procedure.Handling of change control , Deviation , Batch Failure , OOS , OOT , CAPA , reprocess , rework , market complaints , return goods.Maintenance of control samples & documents related to control samples.Responsible for handling pharmaceutical ERP System like pharma suit.,
Keyskills :
validation documentation qualitycontrol qualityassurance gmp continuousimprovementfacilitation erpsystem wavesolder changecontrol marketcomplaints erp bpr oos oot capa pharma es checks coating control