Experienced in independent instrumental analysis of raw material, in-process samples, finished product, and stability samples of pharmaceutical products.
Well versed in analysis of tablets, capsules, and liquid samples for common tests such as Assay, Related substances, Dissolution, and preservative content analysis as per controlled specifications and methods of analysis.
Should be able to operate, calibrate, and maintain instruments like HPLC, GC, Dissolution apparatus, UV, and FTIR.
Experience with Empower and Lab solution software is recommended.
Exposure to perform AMV or development is preferred.
Aware of online and good documentation practices.
Should have knowledge of Data integrity and QMS.
Should be able to maintain cGMP and safety throughout the activities done in the laboratory.