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.
Audit exposure in USFDA/ EUGMP approved company. Exposure of Material Handling / Electronic Batch Record filling and review / Good Knowledge of SAP System & Their T Codes for PPPI / Machine Alarms handling / QMS / Deviation / Change Control / SOP / Daily Reports Preparation/ Manpower Handling.