Support maintenance of the Dutch WDA license in collaboration with the external RP service provider. Ensure all documentation required for WDA compliance is complete, current, and accessible.
Experience in analysis of RM/Finish/ln Process/Stability samples by using instruments like HPLC, UV, Dissolution apparatus, GC, IR and AAS and Documentation related to QMS.
Dissolution apparatus, GC, IR and AAS and Documentation related to QMS. To review respective GMP Documents of QC department such as analytical / worksheet of In Process and Finished Product.
Cadila Pharmaceuticals is an Indian multinational pharmaceutical company based in Ahmedabad. The company's operations focus on manufacturing products ranging from active pharmaceutical intermediates.
Trigger out of specification investigations upon detection of test results outside predefined specifications. Design and execute tests to confirm or rule out suspected root causes.