Alembic Pharmaceuticals is looking for competent personnel to be an integral part of our team for USFDA approved API plant-based at Karakhadi near Vadodara (Guj).
- Review of TTD, ADL Specification, and Analytical Method Validation Report.
- Evaluation of CAPA & its effectiveness.
- Preparation of Specification and STP for In-Process, Intermediate, FP, RM, PM, Cleaning, Recovered Solvent, Skip Testing as per regulatory requirement.
- Preparation of Test Data Sheet for Intermediate, FP, RM, PM, Stability, Recovered Solvent, Skip Testing.
- Initiation of Change Control and its closure.
- Impact Assessment / Risk Assessment.
- Creation of Mater for Specification in SAP.
Those who match the above criteria and are eager to build their career with us can apply at email@example.com
Qualification: B.Sc/B.Pharma, MS/M.Sc/M.Pharma
Experience: 5-7 Years