Virendra Sood

I’m a biopharmaceutical manufacturing professional, building end-to-end GMP readiness through batch execution, documentation, and continuous improvement. I focus on getting the details right—change controls, deviations, and quality risk thinking—so manufacturing runs reliably.

At Intas Biopharmaceuticals, I’ve worked in the Manufacturing Department as an Executive, supporting commercial and engineering work across multiple biologics. I managed commercial batches of molecular antibodies (Rituximab, Bevacizumab, Denosumab) and executed Etanercept drug substance manufacturing, while also supporting EU GMP execution for Filgrastim (100+ commercial batches).

In validation and lifecycle activities, I draft and initiate change controls, quality risks assessments, deviations, and CAPA in QEdge and SAP. I prepare Batch Manufacturing Records, Process Qualification (PQ/PV) and Process Performance Qualification (PPQ) protocols and reports, including impact assessments and CAPA closure reports, and I compile equipment qualification documents (URS, PQ, DQ, RQ).

I also bring strong downstream processing familiarity, including chromatography, column packing, and Tangential Flow Filtration (TFF) using AKTA systems and related equipment checks. I’m proud of recognition like an INTAS Spot Award (August 2023), and I enjoy improving processes through structured systems, disciplined execution, and practical learning.