Regulatory Affairs Specialist
Ghalioungui
Employer Active
Posted on 15 Dec
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Experience
1 - 3 Years
Education
Bachelor of Science, Bachelor of Pharmacy(Pharmacy)
Nationality
Any Nationality
Gender
Not Mentioned
Vacancy
1 Vacancy
Job Description
Roles & Responsibilities
Responsibilities:
- Ensure full compliance with EDA regulations governing medical device registration, listing, importation, and post-market activities.
- Interpret and apply national regulatory requirements, including guidelines and circulars issued by the EDA.
- Develop regulatory strategies tailored to Egyptian market timelines and requirements.
- Support internal teams by providing clear regulatory guidance for product development, labeling, and market introduction.
Regulatory Submissions (Egypt)
- Prepare and submit dossiers for medical device registration to the Egyptian Drug Authority, including required administrative, technical, and quality documentation.
- Manage the device classification process based on EDA rules.
- Coordinate with EDA officials regarding inquiries, follow-up requests, inspections, or clarifications.
- Maintain valid registrations and ensure timely renewals, updates, and import license approvals.
Documentation & Quality Compliance
Support auditing processes and regulatory inspections.
Desired Candidate Profile
Bachelor s degree in Pharmacy, Biomedical Engineering, Biotechnology, Life Sciences, or related field.
1 2 years of regulatory affairs experience in the Egyptian medical device industry.
Experience dealing directly with EDA submissions and systems (such as device listing, import license, or registration platforms) is strongly preferred.
Company Industry
- Medical
- Healthcare
- Diagnostics
- Medical Devices
Department / Functional Area
- IT Software
Keywords
- Regulatory Affairs Specialist
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