Regulatory Affairs Specialist

Company Description

SuLinda is a prominent multinational company specializing in full product development and supporting healthcare organizations to access the Saudi and Gulf markets efficiently. SuLinda provides a comprehensive range of products and services tailored to meet the needs of diverse business owners aiming for business readiness in these regions. As a leader in business consulting and advisory services, the company offers a unique product portfolio and operates from offices in Saudi Arabia, Poland, and Egypt. SuLinda is committed to driving success for businesses within the Gulf region with its expertise and dedication.

Role Description

This is a full-time on-site role for Export Regulatory Affairs Specialist, located in Cairo, Egypt. The specialist will be responsible for preparing, reviewing, and submitting regulatory documentation, ensuring compliance with relevant regulations, and managing regulatory submissions. Additional responsibilities include staying abreast of evolving regulatory requirements, liaising with relevant authorities, and collaborating with internal teams to achieve regulatory compliance.

Qualifications

• Bachelor's degree in Pharmacy, biotechnology, Vet, or a related field
• 12 years of experience in food supplement registration in KSA and UAE markets.
• Strong skills in Regulatory Documentation, including preparation and review of documents for accuracy
• In-depth understanding of Regulatory Compliance and adhering to Regulatory Requirements
• Demonstrated ability to stay updated with evolving regulatory landscapes
• Exceptional attention to detail and organizational skills
• Strong communication and team collaboration capabilities