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Manager - QC
Piramal Pharma
posted 3d ago
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Job Description
- 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)
Employment Type: Full Time, Permanent
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