Desired Profile:
1. Candidate should have sound experience ofI Injectableparenteral /sterile Manufacturing
2. Production planning & target achievement inI Injectable& Lyophilisation Dept.
3. Production and Planning for Batch wise release.
4. Maintain the record as per the GMP & regulatory requirement
5. Handling of qualification document of equipmenta and area qualification.
6. Taken an active part in validation activities of vial washing Autoclave, tunnel, and aseptic process simulation.
7. Preparation of SOP and review of the SOPs of ther respective areas.
8. Reviewing of a documents and the compilation of the documents, preparation & review of Documentsl likeBMR & BPR, Qualification:s
9. Preparation of process-order.
10. Please do not apply if you are from API and other than pharma background
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