<ul><li>Lead the QA team in managing quality systems including deviation handling, CAPA, change control, and risk assessments</li><li>Ensure implementation and compliance with cGMP, GLP, ICH, WHO, and regulatory authority requirements</li><li>Oversee batch record review, product release, and document control activities</li><li>Coordinate and face regulatory audits (USFDA, MHRA, TGA, WHO, etc.) and customer audits; ensure audit readiness</li><li>Monitor the execution of internal audits and track audit observations to closure</li><li>Review and approve SOPs, qualification protocols, validation documents, and master documents</li><li>Ensure proper documentation practices (GDP) across departments</li></ul>

Manager/Sr. Manager-QA (IPQA)