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:
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Regulatory Compliance - Ensure all products meet international regulations, serving as the primary regulatory contact for our international hubs
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Product Registration - Prepare, submit, and manage dossiers for new drugs, renewals, and variations, guiding approvals from start to finish
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Compliance Monitoring - Stay ahead of evolving regulations, advising internal teams on critical updates to maintain full compliance
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Labeling & Packaging Review - Ensure all pharma labeling, packaging, and promotional materials adhere to regulatory standards
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Cross-Functional Collaboration - Partner with R&D, QA, Manufacturing, and Marketing to embed regulatory requirements at every stage
Qualifications:
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Bachelor's degree in Pharmaceutical Sciences
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+2 years of experience in Regulatory Affairs in international Markets.
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Fluent in English (written & verbal) - essential for global collaboration
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Detail-oriented, proactive, and eager to grow in a dynamic regulatory landscape