Regulatory Affairs Specialist
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 international regulations, serving as the primary regulatory contact for our international hubs.
- 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.
Qualifications:
- Bachelor’s degree in Pharmaceutical Sciences.
- +2 years of experience in Regulatory Affairs in international Markets.
- Fluent in English (written & verbal) – essential for global collaboration.
- Detail-oriented, proactive, and eager to grow in a dynamic regulatory landscape.