Responsible for Analytical Method Development of Assay.
Responsible for routine, finished product and stability sample analysis for various markets such as IRF, ROW and WHO etc.
Responsible for Content Uniformity & Blend Uniformity related substances, Dissolution, Residual Solvents for Drug Product.
Responsible for Analytical Method Validation for Drug Product I.e. Designing Method Validation Protocol, TDS Preparation and planning method validation study as per protocol for various markets.
Responsible for Technology Transfer at Plant Location (Designing Protocol for Technology Transfer to Q.C and Execution through collaborative study and troubleshooting if any)
Responsible for Pr-formulation study support for formulation development.
Responsible for preparation of Standard Test Procedures (STP) & Specification.
Responsible for Calibration of various Analytical Instrument (HPLC, GC, UV, Dissolution apparatus, Weighing Balances, Kf Autotitrator, ph meter, Osmometer, and Viscometer)
Salary 2.75,000 to 4.50,000 PA
Experience1 year - 5 year
INDUSTRYPharma , Biotech , Clinical Research