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.

More than 2 years of experience in regulatory affairs in the Egypt market.

Fluent in English (written and verbal) – essential for global collaboration.

Detail-oriented, proactive, and eager to grow in a dynamic regulatory landscape.