Technical Supervisor

• Ensuring GLP compliance & Analysis of FP/In process/Validation/Raw Material samples in Penicillin QC lab, Dholka. • Ensuring GLP compliance & Analysis of FP/In process/Validation/Raw Material sample, Stability and Raw Material sampling in Penicillin QC lab, Dholka. • To ensure the compliance of GLP in Quality Control Lab. • To analyze the finished products, In-process and Raw Material sample by chemically / instrumental method. • To receive the samples for analysis and making entry in Inward register. • To maintain the Instruments log books related to FP analysis. • To analyze the validation sample and compilation of documents. • To enter the finished product results through LIMS. • Follow cGMP in Laboratory. Responsible for online documentation. • Responsible for taking of Continuations sheet (CS) and print out Record of analysis (ROA) through LIMS.

Cadila Pharmaceuticals