Regulatory Affairs Specialist
Eva Pharma
| Company | Eva Pharma |
| Category | Legal & Compliance |
| Location | Giza |
| Remote | On-site (inferred) |
| Employment | Not stated |
| Level | Not stated |
| Salary | Not stated by the employer |
| Posted | 4 Jun 2026 |
| Last verified | 10 Aug 2026 |
| Source | Employer ATS (workable) |
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.