Chandresh Tiwari

I am writing to express my strong interest in the Quality Control leadership opportunity at your esteemed organization. With over 20+ years of progressive experience in the pharmaceutical industry, I bring a robust background in analytical operations, regulatory compliance, and quality systems management across both formulation and API sectors. In my current role as Director – Quality Control at Vibonum Technologies (Althera Group), I have successfully established fully operational QC and microbiology laboratories from greenfield stage for oral solid dosage manufacturing. My responsibilities include oversight of analytical instrumentation (HPLC, GC, UV, IR, TOC), method validation, LIMS integration, regulatory audit readiness (USFDA, MHRA, WHO-GMP), and cross-functional coordination to ensure timely batch release and compliance. Prior to this, my tenure at Baxter Pharmaceuticals, Medreich, Wockhardt, Ranbaxy laboratories, Cipla labs, Sun Pharmaceuticals and other leading firms helped me hone critical skills such as CAPA and deviation handling, risk-based vendor qualification, and digital transformation of QC operations using platforms like SAP, JDE Edwards, Trackwise, Veeva vault and LIMS. My contributions have been recognized twice with the Baxter ‘Star of the Year’ award for driving cost-effective and compliant improvements and WOCK -Star Awards in Wockhardt for my significant Contribution . I am confident that my strategic thinking, operational expertise, and dedication to quality excellence make me a strong fit for your organization. I welcome the opportunity to further discuss how I can contribute to your quality objectives. Thank you for considering my application. I look forward to your response. Warm regards, Chandresh Kumar Tiwari .