Global Regulatory Affairs Manager

Company DescriptionNAPCO PHARMA is an Egyptian pharmaceutical company with a portfolio of over 350 products spanning all therapeutic areas. Operating from a state-of-the-art GMP and ISO certified manufacturing facility in Egypt, the company is dedicated to delivering high-quality pharmaceuticals at competitive prices. NAPCO PHARMA exports its products to 15...

**Introduction to role**: Are you ready to be part of the team of Regulatory affairs for Near East & Maghreb Countries markets? As the Regulatory Affairs Lead, you'll ensure AstraZeneca's "License to Operate" regulatory activities are met for all products, aligning with Near East & Maghreb Countries markets legislation and our code of "Good Regulatory...

Seeking a Strategic Head of Regulatory Affairs with RecentSaudi Food and Drug Authority (SFDA)ExpertiseKey Highlights of Recent Experience:Leads end-to-end regulatory activities for a broad portfolio including  human pharmaceuticals, health products, food supplements, cosmetics, and medical devices  in full compliance with SFDA standards.Provides...

**Job Function**: Regulatory Affairs Group **Job Sub Function**: Regulatory Affairs **Job Category**: Professional **All Job Posting Locations**: Cairo, Egypt **About Innovative Medicine** Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that...

Job ObjectiveRegulatory Affairs Specialist is responsible for assisting in obtaining and maintaining National Health Authorities (EDA) and International approvals (as required) for Plasma supply chain facilities, products Manufacturing Facility, Plasma Exportation and finished product importation and release.Key responsibilityPrepare and submit all...

_Advance healthcare with IQVIA - where your expertise drives innovation and compliance._ **About the Role** As a Senior Regulatory Affairs Coordinator at IQVIA, you will play a critical role in ensuring regulatory compliance and supporting submissions of Cosmetics, Nutritional Products, and Medical Devices across Egypt and GCC. You’ll collaborate with...

The Bel Group is a major player in the food industry through portions of dairy, fruit and plant-based products, and one of the world leaders in branded cheeses. Its portfolio of differentiated and internationally recognized brands includes The Laughing Cow®, Kiri®, Babybel®, Boursin® Nurishh®, Pom'Potes® and GoGo squeeZ®, as well as some 30 local...

**Major accountabilities**: - Manages multiple, large and complex local and global regulatory submission projects. - Develop and provide submission and contribute to the technical related regulatory strategy, intelligence and knowledge required to develop, register, and maintain local and global products. - Contribute to strategic and technical...

Company DescriptionKemet Medical, a 40-year-old medical equipment company, is dedicated to providing innovative, high-quality healthcare technologies combined with exceptional customer service to empower caregivers in enhancing patient lives. Over the years, we have grown from a small team of 10 employees to a thriving organization of over 150 team members,...

**- Organizes submission plans on all products for assigned countries. - Implement the agreed regulatory strategy regarding new products and maintain products licences in the allocated countries. - Be part of the team planning the strategy for regulatory activities for the allocated countries - Do the submission compilation, publishing and approval...