Global Regulatory Affairs
New Cairo, Cairo
Global Regulatory Affairs
New Cairo, CairoPosted 26 days ago34Applicants for1 open position
- 4Viewed
- 0In Consideration
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Job Details
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Job Description
- Register global product and approvals, including compiling and submitting regulatory dossiers.
- prepare and review of technical documents (e.g., ingredient specifications, label claims, safety assessments).
- Liaise with regulatory authorities to facilitate product approvals and address queries.
- Review product labels, packaging, and promotional materials to ensure compliance with regional regulations.
- Monitor and communicate changes in global regulatory requirements relevant to dietary supplements.
- Assist in keeping company informed of regulatory requirements and external standards in international markets.
- Prepare International submissions and obtain product approval/clearance to include assistance with government queries and registration documentation requirements.
- Review Change Orders and assess regulatory impact of product changes on International regulatory strategy and submissions per standard procedures.
- Support post market regulatory compliance activities for international product approvals.
- Advise internal stakeholders (R&D, Marketing, Quality, Legal) on regulatory requirements affecting product development and marketing.
Job Requirements
- Bachelor's Degree in Pharmaceutical Sciences, Nutrition, Science, or a related field.
- Experience in Dietary Supplements is a plus.
- Minimum of 3-6 years of regulatory affairs experience.
- Fluent of English language written & spoken.
- Strong understanding of regulatory frameworks, product registration processes, and labeling requirements.
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