Saud Alqahtani

• Lead and manage regulatory submissions, variations, renewals, and new registrations across KSA and the cluster region.
• Follow up on all types of regulatory requests and requirements with SFDA and GHC to ensure timely approvals and updates.
• Coordinate and maintain regular communication with regulatory stakeholders within SFDA and GHC.
• Develop and strengthen strategic relationships with key personnel within health authorities to ensure proactive engagement and mutual understanding.
• Act as the key point of contact between the company and government bodies, ensuring transparency, compliance, and timely responses to regulatory inquiries.
• Improve communication channels and build trust to enhance the company’s access and visibility within SFDA, GHC, and other relevant authorities.
• Monitor regulatory changes and assess their impact on the business, ensuring internal stakeholders are informed and aligned.

• Manage all scientific office functions in accordance with SFDA and GHC regulations, including compliance with scientific promotion, product information, and medical affairs standards.
• Serve as the primary liaison between the company and government bodies, including the Saudi Food and Drug Authority (SFDA), Gulf Health Council (GHC), Ministry of Health, and other regulatory and governmental institutions across GHC countries.
• Follow up on all types of requests, submissions, and inquiries with SFDA and GHC, ensuring timely responses and approvals.
• Represent the company in official meetings with authorities and ensure alignment with national and regional regulations and policies.
• Develop and maintain strong professional relationships with stakeholders within health and regulatory bodies to support product access, policy shaping, and regulatory clarity.
• Facilitate communication and coordination between internal departments (Regulatory Affairs, Medical, Market Access, etc.) and external government entities to ensure smooth operations.
• Monitor changes in the regulatory and governmental environment, and proactively communicate implications to leadership and relevant teams.
• Support public affairs strategies that align with the company’s business objectives and regulatory environment in KSA and the region.

• Responsible for overseeing the manufacturing processes of pharmaceutical products to ensure compliance with Good Manufacturing Practices (GMP), quality standards, and regulatory requirements.
• Coordinates production activities, monitors batch records, ensures proper documentation, and supports continuous improvement initiatives to maintain product quality and efficiency.