Posted:-1 days ago|
Platform:
Work from Office
Full Time
• To maintain and adherence of the GLP and safety procedures in laboratory. • To raise the request for issuance of work data sheet / protocols. • To perform the analysis as per work allocation and records the results in work sheet / protocol and maintain on line documentation. • To maintain the CFR 21 part -11 compliance by following laid down procedures. • To perform all the HPLC related analysis of In-process, finished products & returned goods / Hold time / Stability study /reference / working standard analysis as per laid down specification & test procedures , SOPs, as per work allocation and report the analysis data in LIMS modules and report to Section – Head. • To ensure that every specification and method of analysis used of right product/material code. • To report any QI/NQI/OOS/OOT / Deviation/ discrepancy in laboratory analysis to QC- In charge. • Responsible for performing calibration of laboratory instruments as per schedule and laid down SOPs with documentation and updation of instrument calibration status tag. • To record and ensure all the entries and results are in line with current specifications and STPs. • To ensure column performance and column entry are maintain in column logbooks. • To maintain instruments log books properly as per analysis. • To acquire training from concerned person to update the cGMP system update technical knowledge. • To record analytical data in work data sheets / protocols for raw material / packing materials/intermediates/in process/APIs and etc. as per current specification and method of analysis. • To maintain reference / working standard/impurity standard usage records. • To maintain instrument history record. • Joint analysis with R&D personnel during analytical method transfer on HPLC. • To perform analysis of stability samples as per stability schedule.
Cadila Pharmaceuticals
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