Overview
Regulatory Affairs Specialist – Europe Cluster Jobs in Giza, Al Jizah, Egypt at EVA pharma
Title: Regulatory Affairs Specialist – Europe Cluster
Company: EVA pharma
Location: Giza, Al Jizah, Egypt
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 detail-oriented and driven 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:
- Prepare and submit regulatory applications and documentation to the appropriate authorities within Europe
- Review and assess product labeling, promotional materials, and technical documentation for compliance with regulatory requirements
- Maintain knowledge of current and evolving regulations in the pharmaceutical sector, particularly within the European Union
- Act as the liaison between the company and regulatory authorities, facilitating communication and addressing inquiries or issues
- Support the development of regulatory strategies for new product registrations and life cycle management
Requirements
- Bachelor's degree in Pharmacy, Life Sciences, or a related field
- 1-3 years of experience in regulatory affairs within the pharmaceutical or healthcare industry
- Knowledge of EU regulatory frameworks, guidelines, and procedures
- Excellent communication skills, both written and verbal, in English; proficiency in additional European languages is a plus
- Highly organized with the ability to manage multiple projects and deadlines effectively