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Regulatory Affairs Specialist

Eva Pharma

Workable
Location
Giza, El Omraniya, Egypt, Egypt
Type
Not specified
Salary
Salary not specified
Posted
4 Jun 2026
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 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. Key Responsibilities: Regulatory Compliance – Ensure all products meet the Egyptian regulations. Product Registration – Prepare, submit, and manage dossiers for new drugs, renewals, and variations, guiding approvals from start to finish. Compliance Monitoring – Stay ahead of evolving regulations, advising internal teams on critical updates to maintain full compliance. Labeling & Packaging Review – Ensure all pharma labeling, packaging, and promotional materials adhere to regulatory standards. Cross-Functional Collaboration – Partner with R&D, QA, Manufacturing, and Marketing to embed regulatory requirements at every stage. Requireme
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 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. Key Responsibilities: Regulatory Compliance – Ensure all products meet the Egyptian regulations. Product Registration – Prepare, submit, and manage dossiers for new drugs, renewals, and variations, guiding approvals from start to finish. Compliance Monitoring – Stay ahead of evolving regulations, advising internal teams on critical updates to maintain full compliance. Labeling & Packaging Review – Ensure all pharma labeling, packaging, and promotional materials adhere to regulatory standards. Cross-Functional Collaboration – Partner with R&D, QA, Manufacturing, and Marketing to embed regulatory requirements at every stage. Requirements Bachelor’s degree in Pharmaceutical Sciences. +2 years of experience in Regulatory Affairs in Egypt Market. Fluent in English (written & verbal) – essential for global collaboration. Detail-oriented, proactive, and eager to grow in a dynamic regulatory landscape.