With over a decade of dedicated service in the pharmaceutical industry, I am a seasoned Quality Assurance professional with expertise in ensuring the highest standards of quality, safety, and compliance. My extensive experience spans various critical areas, including Batch release , Quality Management Systems (QMS), Process Validation, and In-Process Quality Assurance (IPQA). I am committed to upholding regulatory guidelines, enhancing operational efficiency, and safeguarding product integrity.Key Skills: • Quality Assurance: Proficient in conducting inspections, audits, and risk assessments to maintain pharmaceutical quality standards in alignment with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). • Quality Management Systems (QMS): Experienced in implementing, maintaining, and optimizing QMS frameworks to streamline processes and ensure adherence to rigorous quality standards. • Validation: Expertise in validating pharmaceutical processes and equipment, ensuring compliance with regulatory requirements and industry best practices. • In-Process Quality Assurance (IPQA)& Batch release : Skilled in monitoring and controlling critical stages of manufacturing to promptly detect and address quality issues, contributing to consistent product quality. And also responsible for final batch disposition with all the relavant documents & COA review. • Regulatory Compliance: Profound understanding of pharmaceutical regulations and a proven track record of successful interactions with regulatory authorities. • Problem-Solving: Adept at identifying and resolving quality-related challenges, ensuring timely corrective and preventive actions. • Communication: Strong interpersonal and communication skills, enabling effective collaboration with cross-functional teams and stakeholders.