Regulatory Affairs Specialist
Eva Pharma
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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.
Summary
Ensure product compliance, manage dossiers, monitor regulations, and collaborate across teams
Job title
Regulatory Affairs Specialist
Experience level
2+ years
Minimum experience
2+ years exp
Industry
pharmaceuticals
Location requirements
Giza, Egypt; on-site work required
Salary
Not specified
Management role
No
Required skills
Preferred skills
Specializations
Structured locations inferred from the posting.
Giza, El Omraniya, Giza Governorate, Egypt