Job summary
Regulatory Affairs Intern at Novartis in Riyadh supporting the regulatory team with registration dossiers and lifecycle maintenance. The role offers practical experience in Health Authority requirements, regulatory submissions, product information and compliance through structured projects and coaching.
Key responsibilities
- Support preparation of registration dossiers for new products, extensions and new indications
- Assist with lifecycle maintenance: variations, renewals and safety label changes
- Monitor and summarize national regulatory guideline updates and Health Authority communications
- Track product information updates from submission through approval and assist with artwork
- Maintain data in regulatory information systems and archive regulatory documents
- Keep global trackers and compliance reports up to date per local regulations
- Support preparation and submission of scientific lecture packages
- Assist manager-assigned initiatives while following company SOPs and regulations
Requirements
- Bachelor’s degree in pharmacy (fresh graduate)
- No prior work experience required
- Internship, training or research in regulatory affairs or pharma is an advantage
- General awareness of national Health Authority regulations is an advantage
- Proficiency in English and Arabic
Skills
Regulatory submissionsMicrosoft WordMicrosoft ExcelPowerPointRegulatory databasesDocumentationAttention to detailCommunicationOrganizationCollaboration
Source: Workday. Last checked as open: 13 Nov 2026. You apply directly with the employer.
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