6 - 10 years
5 - 12 Lacs
Posted:6 hours ago|
Platform:
Work from Office
Full Time
1. To undertake literature search & preparation of report for a new development project.
2. To execute development trials as part of prototype development till technology transfer of new drug products at the manufacturing sites.
3. To guide & supervise development trainees or associates during development of new formulations.
4. To prepare Master documents of MFC / MFR / BMR / BPR /PVP / Development reports for submission & validation batches.
5. Material Master creation of Material code/ Vendor code in ERP.
6. MIC creation of Raw material / Packing material / Finished products in ERP.
7. Applying Test / Import / Manufacturer Licenses
8. Involving all Development QA activities & ensure compliance.
M. Pharm/ Ph.D in Pharmacy
Walter Bushnell
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