Quality Documentation Expertise● Lead the implementation of automation for APQR (Annual Product Quality Review)preparation.● Support AI training and validation using real-world pharma quality documents.● Assist in automating documentation related to:○ APQR (Primary)Quality investigations (Secondary)○ Deviations and CAPA (Secondary)○ SOP documentation (Secondary)○ Quality reports and summaries (Secondary)experience5

Key responsibilities:Oversee daily operations, manage personnel, and provide technical andstrategic direction for the QC department.Develop, implement, and maintain quality control systems and ensure allprocesses adhere to company standards and regulatory requirements.Supervise the analysis of raw materials, in-process samples, finishedproducts, and stability samples. Review analytical data, protocols, andreports. Thorough knowledge in handling all