Executive
1 month ago
**Date**:Mar 19, 2024
**Location**: Pithampur, MP, IN
**Company**:Lupin
**_Position - Executive -QA_**
**_Expereince - 5 to 10 Years_**
**_Education - B. Pharma_**
**_Note : Regulatory exposure is madnatory.i.e USFDA._**
- In-process Quality Assurance during production activity including line clearance and sampling at different stages of Processing /Packing as per the requirement - MDI/DPI/DERMA.
- Review of Master Documents such as BMR/BPR, Test batch monitoring protocols / process validation protocol and reports, equipment qualification documents.
- Swab/Rinse sample collection of production equipment.
- Review of executed BMR/ BPR/ Logbooks, investigation reports. Preparation of trends Deviation, IP-OOS, Change Control, Market Complaint, CAPA.
- Review of executed batch records, preparation of QA SOPs.
- Visual Examination of FP control sample, preparation of hold time study protocol.
- Review of equipment CSV documents.
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