Regulatory Affairs Specialist - Europe Cluster
- Giza
- Permanent
- Full-time
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.
- 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.