Zahrawi Group is a leading company in the GCC Healthcare Industry with its presence in UAE, KSA, Qatar, Bahrain, & Oman markets. The company supplies and distributes high-quality products and services to Hospitals, Clinics, Laboratories, & Analytical Industries.
The incumbent is responsible for all Product Classification/Manufacturing Site Registration and Product Registration and to ensure that all documents required are available and are submitted on time.
They are also responsible for the preparation of the pre- and final permits for the imported items as per the SFDA guidelines.
ACCOUNTABILITIES
Policies & Procedures:
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Adhere to all Zahrawi Policies & Procedures as applicable.
Regulatory Affairs:
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Ensure that Zahrawi’s products comply with the regulations of the SFDA.
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Keep up to date with the latest changes in regulatory legislation and guidelines.
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Liaise and negotiate with regulatory authority to ensure a smooth registration process.
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Provide advice about regulations to customers/suppliers.
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Analyze product complaints and make recommendations to solve the problem and to avoid them in the future.
Product Classification & Registration:
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Ensure that all required documents and actions for Product Classification/Manufacturing Site Registration and Product Registration are available.
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Prepare all required documents to be submitted for Product Classification under SFDA.
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Prepare all required documents to be submitted for Manufacturing Site registration under SFDA.
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Prepare all the Dossiers to be submitted to SFDA for medical, pharmaceuticals and GSL products.
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Prepare and submit samples to SFDA for product registration completion.
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Collect all necessary documents from Supplier to submit for SFDA of products under Ghad System.
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Register reagents with restricted elements through Ghad System.
Importation Permits:
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Prepare and apply for the pre-permit document as per the SFDA guidelines and verify the items being imported and the documents required.
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Apply for the MOH Narcotics and Pre-cursor Chemical permits on the SFDA website as per the specified guidelines.
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Register and submit the permits through Ghad system.
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Resubmit any permits that have not been approved and make sure all the information provided is correct and attach any new documents if required.
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Prepare weekly / monthly report regarding the rejections/ delays for SFDA importation permits and reasons related to that.
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Check and review the safety data sheet of the restricted element to prepare the required documents for obtaining MOI approval.
Exportation Permits:
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Prepare the required documents necessary for obtaining SFDA approval to export medical products outside KSA.
Importation Rules & Regulations:
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Communicate with the existing and new suppliers regarding SFDA importation rules and policies.
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Upload on the SFDA importation system any new classifications or registration certificates.
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Ensure that all urgent request from the Sales team and suppliers are dealt with in a fast manner and ensure that all documents are in place.
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Report any deviation from SFDA guidelines of imported shipments and take the corrective and preventive action accordingly.
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Review on a regular basis the SFDA importation process of distribution agreements.
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Ensure that the SFDA license is renewed before expiry date to avoid importation disturbance.
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Segregate the imported products as per HS code in coordination with logistic team and confirm if products are SFDA regulated or not.
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Coordinate with the Procurement & Logistics Team to update all the required documents in time to avoid importation rejections.
Audit:
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Prepare any documentation needed for internal and external audits.
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File all documents in the corresponding files to ensure all are available and are correct.
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Evaluate the suggestions after the audit and implement them when possible.
Admin:
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Assist the Warehouse Coordinators with relevant documents when requested.
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Coordinate with the Procurement team and assist them with any question they or the Suppliers may have related to SFDA importation.
Note: Zahrawi employees must step into other work assigned to them as business needs arise and are not limited to the above.
REQUIREMENTS
Education: Bachelor’s degree (Biology/ Pharmacy/ Biomedical or Science related major is an advantage)
Experience: 2-3 years of relevant experience in regulatory affairs
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Job Specific Skills: Effective Communication skills & Good English - Time management skills - Problem Solving Skills - Good computer skills in Ms. Office (Excel– ERP/Oracle system) – Process Management skills – Detail Oriented – Knowledge about Saber System & Ghad System - Knowledge in SFDA regulations.
Additional Details: Candidate should be Saudi National and based in Riyadh, KSA.
Location: KSA - Riyadh
Job Type: FULLTIME
Job Posting Date: 03-09-2025
Division/Department: Regulatory Affairs and Pharmacovigilance