Head of Regulatory Affairs

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...

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...

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,...

The Regulatory Affairs Specialist will be primarily responsible for managingimportation approvalsfor medical devices and consumables — ensuring full compliance with EDA regulations and supporting in registration, vigilance, variation, controlled release, inspection and compliance.Key Responsibilities:Obtain importation approvals from regulatory...

: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 countriesDo the submission compilation, publishing and approval information processes...

Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.  Job Summary:We are seeking a passionate and talented Regulatory Affairs...

Job DescriptionPrepare, compile, and submit registration dossiers for new products (human medicines, medical devices, or cosmetics as applicable) to the health authorities.Handle product renewals, variations, and post-approval changes according to regulatory timelines.Ensure regulatory compliance of product labeling, artwork, and promotional...

Job Title: Regulatory Affairs Specialist Submission Assembly Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge...

Job Title: Regulatory Affairs Specialist Submission AssemblyBusiness IntroductionAt GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology...

SC JOHNSON IS A FIFTH-GENERATION FAMILY COMPANY BUILT ON THE SPIRIT OF OUR PEOPLE. We have been leading with purpose for over 130 years, building iconic brands that win the hearts and minds of consumers – such as Raid, Glade, Ziploc and more, in virtually every country around the world. Together, we are creating a better future – for the planet, for...