CQA Executive

ERP Management: Create and update Bill of Process (BOP) entries for in-house and loan license (LL) manufacturing sites. Generate and revise Item Master Codes for packaging materials and finished goods. Maintain ERP item master update records as per Format No. QAD-FR-89. Raw Material Specification (RMS): Prepare and revise RMS documents in line with regulatory and internal requirements. Draft RMS for product registration, including compliance with UK market norms. Finalize and issue authorized RMS for submission to regulatory bodies. Sample Coordination & Analysis: Coordinate dispatch of AVD raw material and NPD samples for lab testing. Maintain records of sent samples in Format No. QAD/FR-42 and ensure timely follow-up for results. Working Standards Management: Arrange and distribute working standards for LL sites in coordination with concerned departments. Artwork Review: Review packaging artwork for: Domestic (Drugs and Foods) Export (Drugs and Foods) Products requiring artwork for regulatory registration Export Documentation: Review Certificates of Analysis (COAs) for export-bound raw materials. Coordinate with external labs (e.g., Precise Lab) to rectify discrepancies and ensure final approval. Destruction Certificates: Share approved destruction certificates with applicable manufacturing sites. Quality Management System (QMS) Documentation: Circulate QMS-related documents such as: Commercial deviations Change control authorizations Document Revisions: Revise Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) for domestic products. Safety & Analytical Documentation: Prepare Material Safety Data Sheets (MSDS) for relevant materials/products. Revise Method of Analysis (MOA) for finished products in coordination with stakeholders.