Piramal Pharma Ltd
Designation : Senior Executive
Function : Quality Control
Functional Area : QC
Job Role Summary : Analysis of QC samples, Method development, validation
Job Profile :
- Analysis of in process, intermediate, raw material, packaging material, ETP and utility samples, stability samples, R&D samples and other samples as per plant requirement as per defined STP’s.
- 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 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.
Job Requirements :
- 6 to 8 years experience in Pharma QC laboratories
Work / Job Experience : 6-8 Years
Type of Experience : Pharma QC experience
Academic Qualifications :
CTC : 6-8 lpa
