Regulatory Affairs Specialist

Regulatory Affairs Specialist

Eva Pharma · Giza, Egypt · — · Posted 2026-06-04

Workplace: on_site

Department: Regulatory Affairs

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.

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.

Apply

Apply at Eva Pharma

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