Highly skilled Pharmaceutical Quality Assurance Specialist with a strong background in ensuring compliance with cGMP, FDA, and ISO standards within pharmaceutical manufacturing environments. Experienced in conducting quality audits, overseeing documentation processes, and implementing corrective and preventive actions (CAPA) to uphold product integrity. Proficient in batch record review, quality risk management, and cross-functional collaboration to ensure regulatory compliance and operational excellence. Adept at problem-solving and driving continuous improvement initiatives to enhance overall quality systems and patient safety.