We are seeking a detail-oriented and experienced Regulatory Affairs Specialist to join our dynamic team. The ideal candidate will play a critical role in ensuring that our products comply with all regulatory requirements, both locally and internationally. This position involves close collaboration with various departments to achieve compliance and support the company's strategic goals.
Key Responsibilities:
- Regulatory Compliance: Ensure that all products comply with local and international regulations, including ingredient safety, labeling requirements, and marketing claims.
- Documentation: Prepare, review, and submit regulatory documents, including product dossiers, safety data sheets (SDS), and product information files (PIF).
- Regulatory Submissions: Manage regulatory submissions and approvals for new products and changes to existing products.
- Regulatory Intelligence: Monitor and interpret regulatory guidelines, standards, and legislation to keep the company informed of new or changing requirements.
- Cross-Functional Collaboration: Work closely with the R&D, Quality Assurance, and Marketing teams to ensure regulatory compliance throughout the product development lifecycle.
- Audits and Inspections: Prepare for and manage regulatory audits and inspections, providing documentation and responses as required.
- Training and Support: Provide regulatory training and support to internal teams, ensuring understanding and compliance with regulatory requirements.
Qualifications:
- Education: Bachelor's degree in Pharmacy, Chemistry, Biological Sciences, or a related field.
- Experience: Minimum of 3-5 years of experience in regulatory affairs in the cosmetics or pharmaceutical industry.
- Knowledge: In-depth understanding of local and international cosmetic regulations
- Skills: Strong analytical, organizational, and communication skills. Attention to detail and ability to manage multiple projects simultaneously.
- Language: Proficiency in English and Arabic
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