34 Job openings found

1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 5.00 LPA
Test to a high, and continuously improving, level of GMP/GLP compliance to ensure patient safety and to minimize risk to the company business   Perform routine testing and basic GMP paperwork review with supervisor direction   Oversee the development and tracking to a plan for day-to-day testing activities to meet the daily manufacturing and ...
4 Opening(s)
2.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 5.00 LPA
Good analytical hand Well experienced in wet chemical analysis Hands-on experience of GC/HPLC/UV preferred Aware of Good Manufacturing and Good Laboratory practices Well versed with documentations related to a pharma laboratory.   Good analytical hand Well experienced in wet chemical analysis Hands-on experience of GC/HPLC/UV preferred Aware of Good Manufacturing and Good Laboratory practices Well versed with documentations related to ...
2 Opening(s)
1.0 Year(s) To 4.0 Year(s)
2.00 LPA TO 3.00 LPA
Good analytical hand Well experienced in wet chemical analysis Hands-on experience of GC/HPLC/UV preferred Aware of Good Manufacturing and Good Laboratory practices Well versed with documentations related to a pharma laboratory.   Good analytical hand Well experienced in wet chemical analysis Hands-on experience of GC/HPLC/UV preferred Aware of Good Manufacturing and Good Laboratory practices Well versed with documentations related to ...
2 Opening(s)
1.0 Year(s) To 4.0 Year(s)
2.00 LPA TO 3.00 LPA
Good analytical hand Well experienced in wet chemical analysis Hands-on experience of GC/HPLC/UV preferred Aware of Good Manufacturing and Good Laboratory practices Well versed with documentations related to a pharma laboratory.   Good analytical hand Well experienced in wet chemical analysis Hands-on experience of GC/HPLC/UV preferred Aware of Good Manufacturing and Good Laboratory practices Well versed with documentations related to ...
4 Opening(s)
2.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 5.00 LPA
Good analytical hand Well experienced in wet chemical analysis Hands-on experience of GC/HPLC/UV preferred Aware of Good Manufacturing and Good Laboratory practices Well versed with documentations related to a pharma laboratory.   Good analytical hand Well experienced in wet chemical analysis Hands-on experience of GC/HPLC/UV preferred Aware of Good Manufacturing and Good Laboratory practices Well versed with documentations related to ...
4 Opening(s)
4.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
To issue the Batch Manufacturing Record, Equipment cleaning record, Logbooks, Analytical Report for raw material, finish product and packing material. Assistance in preparation of SOP of various departments/ preparation of draft SOPs. During plant round QA Executive to verify documents as per cGMP and GLP norms. Line Clearance activities for manufacturing and packaging ...
4 Opening(s)
2.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 5.00 LPA
Good analytical hand Well experienced in wet chemical analysis Hands-on experience of GC/HPLC/UV preferred Aware of Good Manufacturing and Good Laboratory practices Well versed with documentations related to a pharma laboratory.   Good analytical hand Well experienced in wet chemical analysis Hands-on experience of GC/HPLC/UV preferred Aware of Good Manufacturing and Good Laboratory practices Well versed with documentations related to ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 5.00 LPA
? Analysis of RM, PM, IP , FG, Returns & Recalls samples and prepare approvedor rejected test report, monitors QC on-going activities with respect to definedSOP/STP.? Good skills of sampling in gas samples, solid powder, Granules, liquid,semisolid with safe and secure manner.? Knowledge of batch numbering, Packing, Labeling and sealing ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 5.00 LPA
? Analysis of RM, PM, IP , FG, Returns & Recalls samples and prepare approvedor rejected test report, monitors QC on-going activities with respect to definedSOP/STP.? Good skills of sampling in gas samples, solid powder, Granules, liquid,semisolid with safe and secure manner.? Knowledge of batch numbering, Packing, Labeling and sealing ...
1 Opening(s)
14.0 Year(s) To 25.0 Year(s)
20.00 LPA TO 25.00 LPA
Study and identification of synthesis route of assigned projects Synthesis of Chemicals at lab and scale up for pilot scale Development of prototype products and scale up to commercial level Time bound completion of development activities Test method development and characterization of molecules and chemicals Handling of critical analytical instruments like LC-MS, HPLC Day to day ...

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