Regulatory Affairs Manager

Antal International; Riyadh; On-site; SAR 150,000 - 200,000; Full time

Job summary

A leading multinational pharmaceutical company is seeking a Regulatory Affairs Manager/Specialist to oversee SFDA regulatory activities in Riyadh, Saudi Arabia. The role involves managing product registrations, lifecycle compliance, and acting as the liaison with SFD. Candidates should possess a degree in Pharmacy and at least 10 years of experience in regulatory affairs within the Saudi pharma industry, with strong knowledge of SFDA regulations and submissions. Fluency in English and proficiency in Arabic are preferred.

Qualifications

• 10+ years of Regulatory Affairs experience in the Saudi Arabian pharma industry.
• Strong hands-on experience with SFDA regulations and submissions.

Responsibilities

• Lead SFDA regulatory activities for product registrations and compliance.
• Manage new registrations, renewals, and deficiency responses.
• Provide regulatory strategy and support for product development.

Skills

Regulatory Affairs Expertise

Fluent in English

Arabic Proficiency

SFDA Regulations Knowledge

Education

Bachelor's or Master's degree in Pharmacy

Job description

Our client, a leading multinational pharmaceutical company, is looking to hire a Regulatory Affairs Manager / Specialist for their operations in Riyadh, Saudi Arabia. (Saudization)

Job Title: Regulatory Affairs Manager/Specialist

Reports to: Country Manager

Job Summary

The Senior Manager – Regulatory Affairs will lead SFDA regulatory activities for Saudi Arabia, ensuring timely product registrations, lifecycle management, and ongoing compliance. The role acts as the primary liaison with SFD, PV, and Quality teams across product development, registration, and commercialization.

Key Responsibilities

Regulatory Submissions & Lifecycle Management

• Manage new registrations, renewals, variations, and deficiency responses with SFDA
• Track approvals, handle appeals, and maintain product licenses across lifecycle
• Review and approve labelling, SPC, PIL, and bilingual artworks

Regulatory Strategy & Portfolio Support

• Provide regulatory input on portfolio selection, RLD availability, and filing routes
• Support product development with early regulatory guidance
• Conduct regulatory due diligence for in-licensing and localization projects
• Monitor and communicate SFDA guidelines, circulars, and regulatory updates
• Advise on bioequivalence, biowaivers, exemptions, and complex filings
• Benchmark industry practices and support strategy for complex products
• Act as point of contact with SFDA for submissions, meetings, inspections
• Arrange and participate in pre-submission meetings and inspections
• Provide regular status updates to internal stakeholders
• Support MAH responsibilities, PV coordination, brand name approvals
• Provide input on patents, data exclusivity, tech transfer, and local manufacturing
• Identify SFDA-approved packaging/manufacturing sites

Documentation & Translation

• Oversee Arabic–English translations of dossiers, artworks, and PILs
• Support COPP applications for registrations in other markets

Qualifications & Experience

• Bachelor’s or Master’s degree in Pharmacy
• 10 +years of Regulatory Affairs experience in Saudi Arabia pharma industry
• Strong hands-on experience with SFDA regulations and submissions
• Fluent in English; Arabic proficiency strongly preferred