Description

• Follow cGMP and GMP PRACTICES. • Responsible for charging the stability sample of Finished Product as per SOP. • To follow and maintain stability study schedule. • Pulling out samples from chambers as per the schedule • Maintain all stability chambers daily temperature and humidity monitoring. • To follow safety Procedure in QC department. • Responsible for withdraw the stability sample for analysis as per schedule. • To maintain stability study log book of stability sample. • Responsible for preparation of stability study protocol and maintain all relevant records. • Ensure working of all the stability chambers as per the condition and in case of any problems take the correction action. • Ensure cleanliness of stability chamber. • Preparation of stability samples monthly planner. • Analysis of Stability Samples as per schedule • Maintain all stability chambers daily temperature and humidity monitoring. • Preparation of stability summary of all the products.



• To do any other Work assign by HOD. • Follow cGMP and GLP practices in Quality Control Lab. • To analyze the Sample of stability on non-chromatographic instrument such as FTIR, UV, Dissolution, DT, Hardness etc by following test procedure. • Analysis of Stability Samples as per schedule • To attend the training as per schedule. • To follow safety procedure in QC department. • To receive the samples for analysis and making entry in Inward register. • To maintain the Instruments log books related to sample analysis. • To analyze the sample and compilation of documents. • Responsible for taking of Continuations sheet (CS) and print out Record of analysis (ROA) through LIMS. • Responsible for cleaning & monitoring of laboratory. • Responsible for online documentation. • To do any other Work assign by HOD.

📌 Technical Supervisor (India)
🏢 Cadila Pharmaceuticals
📍 India