Regulatory Affairs Specialist - Cairo, Al Qāhirah, Egypt

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 ...

Role Description · This is a full-time, on-site role for a Regulatory Affairs Specialist based in Cairo, Egypt. The Regulatory Affairs Specialist will coordinate and prepare regulatory documentation, ensure compliance with local regulatory requirements, and facilitate successful ...

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. · ...

Job SummaryWe are seeking a passionate and talented Regulatory Affairs Specialist to join our dynamic team. The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry. · ...

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

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

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. · ...

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. · ...

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

+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. · ...

Role Description · This is a full-time, on-site role for a Regulatory Affairs Specialist based in Cairo, Egypt. The Regulatory Affairs Specialist will coordinate and prepare regulatory documentation, ensure compliance with local regulatory requirements, and facilitate successful ...

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

Arcera is a global life sciences company headquartered in Abu Dhabi, United Arab Emirates. Our purpose is to enable longer and healthier lives while creating sustainable growth. We develop, manufacture, and commercialize a broad range of high-quality innovative and proven medicin ...

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

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. · ...

+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. · ...

This is a full-time on-site role for a Regulatory Affairs Nutrition Specialist located in Cairo, Egypt. · ...

We are looking for an Export Regulatory Affairs Specialist to join our growing team. The ideal candidate will have hands-on experience in food supplements registration, particularly with SFDA requirements. · 1–2 years of experience in Regulatory Affairs · Bachelor's degree in Ph ...