Regulatory Affairs Specialist

🏢 Eva Pharma
📍 Giza, EgyptOn-site
📅 Posted: 6mo ago🔄 Updated: 6mo ago
CV%
✨ AI Summary
Regulatory Affairs Specialist responsible for ensuring product compliance with Egyptian regulations, preparing and managing dossiers for new drugs, renewals, and variations, and guiding approvals from start to finish. The role requires staying ahead of evolving regulations, reviewing labeling and packaging to meet standards, and collaborating with R&D, QA, Manufacturing, and Marketing to embed regulatory requirements across the product lifecycle. Candidates should have a Bachelor’s degree in Pharmaceutical Sciences, at least 2 years of Regulatory Affairs experience in Egypt, and fluent English for global collaboration.
Required Skills
Business, Sales & Management
Project ManagementHR Management
Finance, Legal & Governance
HR ComplianceRegulatory ComplianceRegulatory Affairs
Soft Skills & Professional Competencies
Collaboration
Engineering, Construction & Trades
Packaging
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.
Description
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.
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🎯 Overalli74%
⚡ Skillsi85%
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Ontology Match: 85.0
Matched:✓ Requirements Matching✓ Ontology Skills Mapping
📜 Eligibilityi49%
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Local: 19600%
🏗️ Career Fiti91%
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Seniority: 91.0
📋 Requirementsi67%
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Domain: 67.0
🔥 Motivationi78%
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Title Fit: 78.00