We are seeking a Regulatory Affairs & Quality Assurance Specialist to manage regulatory compliance and quality requirements across the company’s product portfolio. The ideal candidate will have a strong understanding of medications and pharmaceutical products, with experience in pharmaceutical regulatory affairs, quality assurance, and SFDA requirements.
Key Responsibilities
Prepare, review, and maintain regulatory documentation for product registrations, renewals, and submissions.
Coordinate with the Saudi Food and Drug Authority (SFDA) on regulatory matters and follow up on submissions.
Monitor regulatory updates and assess their impact on the company’s products and operations.
Support compliance with Good Distribution Practice (GDP) across product storage, handling, and distribution.
Maintain quality documentation, standard operating procedures, and accurate compliance records.
Support quality audits, inspections, and the investigation of deviations and product complaints.
Coordinate corrective and preventive actions and follow up on their implementation.
Develop a thorough understanding of the product portfolio and its regulatory and quality requirements.
Requirements
3–5 years of experience in pharmaceutical regulatory affairs and quality assurance.
Strong understanding of medications and pharmaceutical products.
Knowledge of SFDA requirements and Good Distribution Practice (GDP).
Ability to quickly understand the company’s product portfolio and related compliance requirements.
Strong attention to detail, organizational skills, and documentation accuracy.
Fluency in Arabic and English.
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