Supervising and leading a team of operators and technicians to ensure efficient and compliant production of injectable medications. This includes assigning tasks, providing guidance, and monitoring performance to achieve production targets and maintain quality standards.
M.Sc, M Pharma, B.Pharma Working in QC analysing. Stability. In process. FP RM sample Handling instruments like HPLC, GC, FTIR, UV, DR, SSA, etc. versatile in handling SAP documentation like preparing STPs and review of analytical hard copies and electronic data
Experience must include analysis of Raw Material, In-Process, finished goods; Stability Testing & Stability sample handling for Tablets, Capsules Handling of HPLC, dissolution & other sophisticated instruments.
Discuss base forecast and bottom up forecasts with sales & marketing team and develop consensus forecast. Upload consensus forecast in system and share with Supply Planning Team