67 Job openings found

Handling BMR- BPR Preparation Filling records as per cGMP RM - PM dispensing Validation Track & Trace Coordination with QA/QC Maintenance Dept, Maintain product quality and process safety Manpower Planning Perform other activities allocated by Production Head     Handling BMR- BPR Preparation Filling records as per cGMP RM - PM dispensing Validation Track & Trace Coordination with QA/QC Maintenance Dept, Maintain product quality and process safety Manpower ...

Description:   Quality Assurance Executive / Sr. Officer/ Sr. Executive Total Experience- 05 -07 Year (Possession – 3 ) Function – Should be from formulation background Area Responsibility – 1. Preparation and review of QMS Document, Execution of process validation, 2. Validation for the tablet / Policy 3. IPQA Instrument Handling . 3 Production Integration ...

Material Selection, Fault finding, troubleshooting, installation & commissioning of Process control systems, Field Instruments, PLC etc. Installation and commissioning of same on actual machine and testing of field components.  Maintenance of PLC systems for Temperature / flow / pressure controls of AHU (Air Handling Unit).  Handle breakdowns of PLC controlled manufacturing machines.  Modification ...

1.0     Packing Activities.       1.1 Packing as per order given by marketing team.     1.2 Ensure Grade wise packing.     1.3 Take packing material for packing which is approved by QA and QC.   2.0    Supervision and Coordination of Shipment.      2.1 Confirm shipment.    2.2 Confirm requirement of packing type.            2.2.1 Ensure availability or minimum ...

1.       * Development of formulations such as Suspension Concentrate (SC), Emulsifiable Concentrate (EC), Coated Granules (GR), Water Dispersible Granules & Spray Dried Granules, (WG). * Actively worked on Innovative and Patentability products. * Patent reading, claims understanding * Validation of recipes of different types of formulations. * Evaluation of Technical ...

1. To perform all the activities of Quality assurance departments. 2. Ensure that SOPs are available for all quality related activities and they are current. 3. Prepare and review all quality assurance related documents such as SOPs, log book, format, etc. 4. Responsible for the Release of the final products. 5. Review batch sheet, ...

Collecting and recording data day to day basis of different trials Compile trial reports Finding vendors for raw material/chemicals Follow up for outside sample testing report/ pending purchase items / vendors for sample/quote Working closely with the development team for planning part Manage testing procedure and validation of new batches Technical content

Responsible for Plant & Utility Instrument Maintenance activity. Responsible for planning to review the SOP, Qualification, Validation, Temperature mapping and other activity. Work permit from respective plants and execute the work as per priority of jobs and type of jobs. Calibration documents review and planning of calibration of instruments. Take trouble shooting action for ...

1. To perform all the activities of Quality assurance departments. 2. Ensure that SOPs are available for all quality related activities and they are current. 3. Prepare and review all quality assurance related documents such as SOPs, log book, format, etc. 4. Responsible for the Release of the final products. 5. Review batch sheet, ...

1. To perform all the activities of Quality assurance departments. 2. Ensure that SOPs are available for all quality related activities and they are current. 3. Prepare and review all quality assurance related documents such as SOPs, log book, format, etc. 4. Responsible for the Release of the final products. 5. Review batch sheet, ...