3 - 5 years
0 Lacs
Posted:1 week ago|
Platform:
On-site
Full Time
1.Literature search/study.
2.Pre-formulation study execution.
3.Market/Innovator/reference product characterization.
4.Execution and documentation of trial batches prototype formulation development.
5.Execution and monitoring of development stability studies.
6.Execution of process optimization/scale-up batches. Technology transfer activities at site.
7.Preparation of documents like BOM, MFR, compatibility study protocol and report, stability study protocol and report, PDR, etc. as per requirements
8.Co-ordination with relevant cross-functional departments/teams
9.Having experience/exposure of formulation development of solid oral, liquid, dry syrup, etc. dosage forms aimed for ROW and domestic market.
10.Should possess experience in handling various equipment's like RMG, FBD/FBP, compression machine, roller compactor, coating
1.Total Years Exp.-
2.Notice Period-
3.Current CTC-
4.Expected CTC-
5.Ready to relocate- Chh. Sambhajinagar, Maharashtra- Yes / No
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