Regulatory Affairs Specialist
1 day ago
**Summary**:
Be the bridge between innovation and patient safety—As a Regulatory Affairs Specialist in Saudi Arabia’s dynamic healthcare landscape, you’ll play a pivotal role in shaping the future of medicine. From ensuring compliance with SFDA regulations to accelerating access to life-saving therapies, your expertise drives both public health and industry growth. Join a mission where precision meets purpose, and every regulation you navigate brings better care to millions.
**About the Role**:
**Major**Accountabilities**
- Maintain, with supervision, the internal DRA database accurate and updated: Dragon/DASA
- Relationships within and outside the company - Develop and maintain good working relationships with other Novartis departments both locally and with Head Office and with third-party vendors.
- With Supervision, Review PPMS and ensure AQWA Launch request are prepared and launched on time.
- With Supervision, ensure full support to Global regulatory compliance initiatives in Saudi.
**Minimum Requirements**
- Pharmacy or related science degree.
- Minimum 1 year of RA Experience in reputable pharmaceutical company.
- Experience handling a portfolio/product and dealing with stakeholder such as SFDA and governmental agency.
- Must be Saudi national.
LI-Onsite
Division
Development
Business Unit
Innovative Medicines
Location
Saudi Arabia
Site
Riyadh
Company / Legal Entity
SAP0 (FCRS = CH024) Novartis Consulting AG
Functional Area
Research & Development
Job Type
Full time
Employment Type
Regular
Shift Work
No
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
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