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Regulatory Affairs Specialist

EVA Pharma • English: C1 • Prescription Drugs • Generic Drugs • 4 months ago

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Salary

≈ $14k – $35k per year (Estimated)

Location

In office (Giza)

Confirmed on the employer's own hiring board on Oct 26, 2026. First seen by Alion on Jun 4, 2026. EVA Pharma scores A on the Alion truth index.

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EVA Pharma

EVA Pharma is an Egyptian pharmaceutical manufacturer headquartered in Cairo, developing and producing medicines in areas such as oncology, neuroscience, respiratory, cardiometabolic disease, anti-infectives, ophthalmology and hepatology. It reports about 5,000 employees, three internationally accredited manufacturing facilities, more than 300 marketed products and six legal entities worldwide, and its group includes the animal health unit EVA Vet Science and the supplement brand Limitless Naturals. It hires product and group product managers, quality control and microbiology specialists, engineers, accountants, key account managers and digital marketing and HR specialists.

evapharma.com • HQ: Cairo, Egypt • Generic Drugs • Prescription Drugs • 1001-5000 employees • Est. 2002

Tech stack of EVA Pharma

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.

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