Process Validation & Cleaning validation Protocol & report preparation & review Technology transfer activity GMP round at other dept (IPQA rounds) Qualification protocol & report preparation & review Perform Internal Audit Perform Internal Audit To prepare the compliance report for the audit carried out customer/CQD on quarterly basis as per the agreed timelines for quality functions. Review of Analytical Specification & method of analysis Review of executed Analytical workshit of IM, FP Handling SAP system & activities related to Release, code to code transfer, creation & change of master inspection, sample deduction, Data provide to SAP support teamfor creation of product code QC related activities such as retension sample management , planning as per sales plan Handling of Returned Goods, Customer complaints, Laboratory Incidents Review of Stability data, charging of stability in SAP system Vendor Management related activiies of CQA RA related queries & Declarations & marketing queries Handling of Change control, Deviation, CAPA, QRM Handling of OOS, OOT & OOC Review Analytical Method Validation/Verification protocol and report & related raw data. Software / CSV Validation Review of Audit Trial

📌 Senior Executive - QA (Maharashtra)
🏢 RPG Life Sciences
📍 Maharashtra