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Pharma Regulatory Affairs Supervisor — Lead SFDA Submissions
Job in
Riyadh, Riyadh Region, Saudi Arabia
Listed on 2026-07-18
Listing for:
MRG
Full Time
position Listed on 2026-07-18
Job specializations:
-
Pharmaceutical
Healthcare Compliance
Job Description & How to Apply Below
MRG is seeking a Regulatory Affairs Supervisor — Pharmaceutical to lead the SFDA registration lifecycle and ensure compliant submissions for pharmaceutical products in the MENA region. Based on-site in Riyadh, you will mentor the registration team and coordinate with cross-functional groups on documentation, strategy, and timelines.
Ideal candidates have 5–7 years of Saudi regulatory affairs experience, including 2 years in supervision, and fluency in Arabic and English.
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