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Active Jobs Found
(Last Updated: Mar 29, 2024)
- 3+ years
- Not Disclosed
- Pithampur, India
- Post Date: Feb 05, 2024
- End Date: Apr 05, 2024
- 3+ years
- Not Disclosed
- Pithampur, India
- Post Date: Feb 05, 2024
- End Date: Apr 05, 2024
Responsibilities Shall worked on API Shop floor / in process QA. (IPQA) activity. ( Example: Line clearance ,In process checks during manufacturing activity, Batch release etc) Able to review Master and Executed Batch Manufacturing record (BMR) and Batch Packaging record (BPR). Also able to review and knowledge DQ/IQ/OQ/PQ Validation documents. Able to review Quality control data and related activity. (Like: Stability protocol/Report, Analytical method validation protocol/Report etc) Having exposure of QMS Activity. (Deviation, APQR, Change control, OOS,OOT) Having exposure of Regulatory Audits.(Like USFDA, EDQM, TGA, KFDA, WHO, ANVISA, ANVIMA etc) Able to review Plant SOPs of all the departments. Plant QA API only. Experience 3 to 4 years Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years of Experience"
- Quality control
- pharmacovigilance
- Regulatory Affairs
- Management