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:
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Regulatory Compliance – Ensure all products meet the Egyptian regulations.
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Product Registration – Prepare, submit, and manage dossiers for new drugs, renewals, and variations, guiding approvals from start to finish.
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Compliance Monitoring – Stay ahead of evolving regulations, advising internal teams on critical updates to maintain full compliance.
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Labeling & Packaging Review – Ensure all pharma labeling, packaging, and promotional materials adhere to regulatory standards.
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Cross-Functional Collaboration – Partner with R&D, QA, Manufacturing, and Marketing to embed regulatory requirements at every stage.
Requirements
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Bachelor’s degree in Pharmaceutical Sciences.
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+2 years of experience in Regulatory Affairs in Egypt Market.
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Fluent in English (written & verbal) – essential for global collaboration.
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Detail-oriented, proactive, and eager to grow in a dynamic regulatory landscape.