via Career pages·Yesterday

Deputy Manager

Cadila Pharmaceuticals

Full-timeOn-siteglp compliancequality controlpreventive maintenanceinstrument calibrationanalytical reportingsop reviewlimsstability analysisvendor qualificationraw material analysisstability sample analysisimpurity record keepingsaptroubleshootingdocumentation reviewmaster data entryteam coordination

Location:Dholka, IndiaType:Full-timePosted:Yesterday

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To ensure the GLP compliance in Penicillin Quality Control Lab.
To ensure all the instruments Preventive maintenance and Calibration as per schedule in Penicillin Quality Control lab.
To plan the analysis and trouble shooting in absence of supervisor.
To review the COA of Finished product/ raw material in LIMS after the completion of analysis.
To review Analytical reports of Vendor Qualification Samples, in process, Stability samples Validation samples.
To review the COA, Standard Test Procedure, SOPs and other master documents. (as per requirement)
To ensure the column usage and record’s of impurities and working standard/ reference standard during Raw Material, Finished Product and Stability sample analysis.
To review the instruments log books related to Raw Materials Finished products and Stability analysis.
To do all the activities as per the instructions of immediate senior as well as management.
To check the documentation of Quality Control Lab. for recording the data entries of finished goods.
Release of Finished Product in SAP.
Preparation in master in SAP.