Regulatory Affairs Specialist at Macro Group

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Job Description

Submission and following-up of registration & re-registration files for the company’s products (local and imported) at EDA& NFSA.Follow-up files at EDA & NFSA until receiving the final registration licenses & approvals needed.Submission files & samples and follow-up the analysis of new products at CADC until receiving the final conformity of the product.Receiving of Free Sale Certificates – GMP Certificates, a copy of the factory license issued by the CAPA.Working closely with the department manager in revising final outer and inner packs data & issuing them from EDA & NFSA .Deputized from Regulatory Affairs Manager to revise final outer and inner packs data & issuing them from EDA & NFSA.

Responsible for the on job training of new employees in the department.Applying the company policies and work for achieving its goals according to the ethics, rules & regulations.Performing any other task assigned by the direct manager related to the field of work.

B.Sc pharmacy ,Vet, ScienceExcellent Microsoft Office skillsDealing with different platforms regulatory affairs regulation awarenessCommunication skills, problem-solving skills and strategic planning skills2 - 4 Years of experience in Regulatory Affairs

Requirements & Qualifications

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Quick Role Summary

Opportunity as "Regulatory Affairs Specialist" at Macro Group located in sheraton on a Full-Time basis, suited for Senior Level candidates. Key details from listing: Submission and following-up of registration & re-registration files for the company’s products (local and imported) at EDA& NFSA.Follow-up files at EDA & NFSA…

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2d ago

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