Director of Strategy Management
Saudi Food and Drug Authority
Total years of experience :17 years, 2 Months
- Develop and review SFDA vision, mission, values and strategic objectives in line with SFDA President and board of directors directions
- Review and update strategic plan, oversee implementation of key initiatives and detailed plans in line with pre-set targets
- Design and ensure enforcement of strategic guidelines for initiatives and plans alignment with overall objectives
- Develop SFDA performance management system including processes, tools and methodologies
- Support departments in setting strategic KPIs and targets and in developing performance management guidelines
- Regularly monitor KPIs and conduct overall performance analysis
- Create and implement change management strategies and plans that maximize employee adoption and usage and minimize resistance
- Record risks/ issues, recommend mitigation and resolution measures
- Observe confidentiality procedures as necessary and create, maintain and track comprehensive change management activities documentation
- Develop necessary tools and systems to monitor and report on initiatives’ implementation progress
- Prioritize projects as per SFDA strategic directions and planning
- Consolidate plans and schedules of all stakeholders involved in the program, and manage master timeline for initiatives implementation
- Analyze projects' KPIs measurement results, budget expenditure and resources utilization ratios
- Supervise the development of key KPIs to be tracked by project managers within projects for performance monitoring while ensuring minimal deviation from targeted KPIs
- Assess and supervise interdependencies between projects to ensure efficiency and progress, and to monitor sudden changes in the project’s goal due to unforeseen changes
- Conduct regular meetings with project team, monitor the submission of progress reports and ensure projects are progressing against set timeline
o Supervision and working on the implementation and designing of the National Center for Medical Devices Information and Research Project (NCMDIR) as well as the Radioactive Products e-system.
o Participating and working on the international technical committee ISO/TC210 “Quality management and corresponding general aspects for medical devices”.
o Worked and supervised the Medical Devices National Registry (MDNR), and working on the Medical Devices Marketing authorization (MDMA).
o Working in Medical devices sector’s Quality Control Department to set and improve the Standard Operating Procedures (SOPs) for all processes within the Executive Management of Radiation Protection and Safety and implementing the ISO9001:2008. Also participating on the internal audit.
o Participated with the steering committee in initiating, planning and development of the SFDA Information and Statistics Center.
Key accounts manager; responsible for developing and maintaining a strong strategic relations with customers.
Working in the service and sales for Baxter infusion pumps.
Graduated with honor distinction degree.