5+

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.

Responsible for review and approval of GMP documents, batch records, deviations, CAPA, change controls, and audit observations for BBM facility.

OSD Granulation, Compression, Coating, Wruster Coating, Capsule Filling. B.PHARMACY/ M.Pharmacy at Aurobindo Pharma

Experience to perform analysis on HPLC instrument for raw material, Finished Products, In Process Sample.

Responsible for BET, MLT, and sterility testing with method validation and investigations, ensuring GLP/GMP compliance, accurate documentation, and equipment adherence.

Partner with leadership to achieve objectives and manage teams, ensuring regulatory compliance and adherence to SOPs and cGMP requirements.

Experience in QC Planning, Trackwise, AMV, Review, OOS, OOT, QMS, LIMS, CAPA, QMS and Risk Assessment QC Analyst (Micro)

B. Sc / M. Sc. (Organic Chemistry I Analytical Chemistry) B.Pharmacy / M. Pharmacy 

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