<ul><li>Implement, maintain, and improve Quality Management Systems &nbsp;in compliance with regulatory requirements.</li><li>Develop and revise Standard Operating Procedures and quality documentation.</li><li>Ensure compliance with regulatory requirements, including FDA, WHO, and other applicable guidelines.</li><li>Oversee process validations, including cleaning, method validation, and equipment qualification.</li><li>Conduct risk assessments and recommend risk mitigation strategies to maintain product quality and safety.</li><li>Review and approve batch manufacturing records (BMR) and batch packaging records.</li><li>Prepare and manage deviation reports, CAPA, and change control documentation.</li><li>Ensure all quality-related documentation is accurate, complete, and audit-ready.</li></ul>

Officer to A.M-Quality Assurance