وظيفة أخصائي الشؤون التنظيمية شاغرة لدى أورينت ميديكال سوليوشن في الرياض

Responsibility

• Prepare, review, and submit regulatory applications, registrations, renewals, and amendments to regulatory
• authorities.
• Ensure compliance with SFDA, MOH, and other applicable healthcare regulations and standards.
• Maintain regulatory licenses, registrations, permits, and approvals.
• Coordinate with manufacturers, suppliers, and internal departments regarding regulatory requirements.
• Monitor changes in healthcare regulations and assess their impact on products and operations.
• Support inspections, audits, and regulatory assessments conducted by authorities.
• Maintain accurate regulatory documentation and records.
• Review product labeling, promotional materials, and technical documentation to ensure regulatory
• compliance.
• Follow up on regulatory submissions and respond to inquiries from regulatory authorities.
• Provide regulatory guidance and awareness to internal stakeholders.
• Strong knowledge of SFDA and MOH regulations.
• Understanding of healthcare regulatory processes and product registration requirements.
• Excellent communication and coordination skills.
• Strong attention to detail and documentation management.
• Analytical and problem-solving abilities.
• Proficiency in Microsoft Office and regulatory systems

Education

Bachelor’s degree in pharmacy, Medical Laboratory Sciences, Biotechnology, Life Sciences, or a related healthcare field

Experience

2 - 5 years 󠄀within the healthcare, pharmaceutical, medical devices, or healthcare services sector.󠄀