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.
The global pharmaceutical industry is undergoing a massive transformation. Moving beyond traditional drug manufacturing, the sector is now driven by biotherapeutics, digital health, data analytics, and patient-centric care models. This shift has created an urgent demand for professionals who not only understand pharmaceuticals but can also lead businesses strategically.
Responsible for BET, MLT, and sterility testing with method validation and investigations, ensuring GLP/GMP compliance, accurate documentation, and equipment adherence.
CIRO Pharma Private Limited plant at Biotech Park Phase III is aimed at manufacturing of Anti-Cancer Drugs for regulatory markets like the U.S.A, U.K, Europe, Canada, and South America.