Posted:2 months ago|
Platform:
Work from Office
Full Time
Analysis of in process, intermediate, raw material, packaging material, ETP and utility samples, stability samples, RD samples and other samples as per plant requirement as per defined STP s. Well versed with advance analytical instrument like HPLC, GC, UV, IR, particle sizer, KF titrator. Calibration of all equipment in QC department as per SOP s. To maintain the records of calibration, working standards, stability data, AMC, outside calibration records, instrument log book, validation report, in process and intermediates test reports as per GLP. To perform analytical method validation as and when required. To perform analytical method development project as and when required. To prepare and update the SOP s and STP s of QC department. To maintain 21 CFR part 11 compliance in the laboratory. To release the in process, intermediates samples within defined time line. To perform the sampling of raw materials, packaging materials as per sampling plan. To report any abnormality in analysis and timely reporting of OOS, incidence, disregard and deviation to the lab supervisor. To maintain calibration inside and outside, AMC and stability samples withdrawal schedule. To follow the instruction of lab supervisor for any specific task. M.Sc (chemistry)
Piramal Pharma Limited
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