5 - 10 years
5 - 11 Lacs
Posted:20 hours ago|
Platform:
Work from Office
Full Time
Role & responsibilities 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. Preferred candidate profile M. Pharm/ Ph.D in Pharmacy Interested Candidates can share their resumes on shikha.mishra@walterbushnell.com
Walter Bushnell
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