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Analysis of raw material / finished goods / packaging material as per In-House or Pharmacopoeia Standards. |
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Preparation of all In-House Reports and Certificate of Analysis. |
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Calibration of Instruments, maintenance of Log books. |
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Preparation of reagent and Volumetric solutions as per testing needs. |
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Maintenance of QC Lab as per GLP Norms. |
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Handling of In-Process Section of Any Pharmaceutical Form. |
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Sampling of API / Intermediates / Finished goods as per GMP. |
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Keeping up to date information of running products in Production Sections and proper co-ordination with Production and QA Departments. |
