Regulatory Affairs Specialist

1 day ago


Riyadh, Saudi Arabia Novartis Full time

**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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