Senior Regulatory Specialist - Cairo

This is a full-time on-site role for a Regulatory Affairs Specialist at our Cairo, · Egypt facility. ...

This is a full-time role for a Regulatory Affairs Specialist based in Cairo. The role includes preparing and reviewing regulatory documentation, ensuring compliance with local and international regulatory requirements. ...

Ceutico Consulting Services is a company that provides regulatory affairs and pharmacovigilance services in Egypt and internationally. The Regulatory Affairs Specialist will be responsible for preparing and submitting regulatory documentation, ensuring compliance with regulatory ...

+To prepare, compile, and submit high-quality regulatory documentation to health authorities to gain and maintain marketing authorizations for the company's products. · ...

This is a full-time on-site role for Export Regulatory Affairs Specialist located in Cairo, Egypt. · Preparing reviewing and submitting regulatory documentation ensuring compliance with relevant regulations and managing regulatory submissions. · ...

This is a full-time on-site position for a Regulatory Affairs Specialist located in Cairo, Egypt. · Preparing and handling regulatory registration and importation approvals. · ...

+2 years of experience in Regulatory Affairs in international Markets. Ensure all products meet international regulations, serving as the primary regulatory contact for our international hubs. · Prepare, submit, and manage dossiers for new drugs, renewals, and variations, · gu ...

We are seeking a passionate and talented Regulatory Affairs Specialist to join our dynamic team. · ...

Deal with NFSA & EDA Regulatory Authorities in Egypt concerning Dietary Supplements. · ...

+Prepare regulatory documentation for Pharmaceutical products and Medical Devices. · +BSc Degree in Pharmacy or related field · Experience as Regulatory Affairs Specialist for human pharmaceutical drugs and Dietary Supplements. · ...

This role involves submission and following-up of registration & re-registration files for the company s products (local and imported), working closely with department managers on various tasks. · ...

ElFagr for Medical devices (EFG) company is looking for Regulatory affairs & Importation specialist. · ...

The Regulatory Affairs Specialist will be responsible for preparing regulatory dossiers for new products variations renewals maintaining detailed records of all submissions correspondence approvals reviewing product labeling leaflets promotional materials staying updated with cur ...

This role involves preparing regulatory documentation for export to various countries. The specialist will ensure compliance with relevant regulations and manage regulatory submissions. · ...

To prepare compile and submit high-quality regulatory documentation to health authorities to gain and maintain marketing authorizations for the company's products. · ...

This Export Regulatory specialist prepares and submits export documentation to regulatory authorities. · ...

To prepare, compile, and submit high-quality regulatory documentation to health authorities to gain and maintain marketing authorizations for the company's products. · ...

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+This full-time position as Regulatory Affairs Specialist involves preparing regulatory registration and importation approvals in Cairo, Egypt. · ...

A global life sciences company seeks a Regulatory Affairs Specialist to enable longer and healthier lives while creating sustainable growth. · ...

We are seeking a passionate and talented Regulatory Affairs Specialist to join our dynamic team. · Regulatory Compliance - Ensure all products meet international regulations. · Product Registration - Prepare, submit, and manage dossiers for new drugs. · ...