As a Product Development Supervisor at Sudair Pharmaceutical Company, I lead the formulation development for various product lines, including solid oncology, cytotoxic, and liquid injectable sterile products. With a Master's degree in Pharmaceutical Technology and 11 years of experience in the pharmaceutical manufacturing industry, I have acquired extensive knowledge and skills in production, QA, QC, validation, and regulatory affairs.My mission is to deliver high-quality and innovative pharmaceutical solutions that meet the needs and expectations of the customers and the market. I am responsible for generating R&D related SOPs, ordering suitable lab scale machinery, registering new products, and supporting the variation process. I also oversee the technology transfer projects and work with professional teams from multi-international companies in different countries. I am proficient in Microsoft To Do, cost estimation, and GCC and FDA guidelines for submission and variation.