

Results-driven Regulatory Officer with extensive expertise in evaluating and ensuring compliance with Good Manufacturing Practices (GMP) within the pharmaceutical industry. Demonstrates a proven ability to review complex regulatory documents, conduct risk assessments, and support quality assurance processes. With certification trainings from WHO Geneva in international GMP standards, with a strong foundation in validation, deviation management, and regulatory coordination. Adept at fostering collaboration with stakeholders, developing policies, and maintaining meticulous documentation to uphold the highest standards of pharmaceutical manufacturing. Committed to leveraging my knowledge and regulatory experience to ensure the safety, quality, and compliance of pharmaceutical products in a dynamic global environment.