Regulatory Affairs Specialist

Overview

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Regulatory Affairs Specialist

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California Greens . California Greens Corp. is a leading pharmaceutical and nutraceutical manufacturer with headquarters in New Jersey, USA, and a state-of-the-art production facility in Sudair City for Industry and Businesses, Saudi Arabia. We are committed to delivering high-quality products across the MENA region. Responsibilities

Lead and manage all Regulatory Affairs activities in Saudi Arabia and the MENA region. Coordinate product registration processes in collaboration with local agents and regulatory authorities. Liaise with the Saudi Food and Drug Authority (SFDA) and other regional regulatory bodies to monitor, follow up, and expedite product (SKU) registrations. Respond to regulatory inquiries and ensure the timely resolution of any issues raised by authorities. Prepare, review, and submit regulatory dossiers and documentation in full compliance with local and regional requirements. Qualifications

Bachelor’s degree in a scientific or medical field (Pharmacy, Chemistry, Biology). Minimum of 3 years of hands-on experience in Regulatory Affairs, specifically with SFDA, within the pharmaceutical or nutraceutical sector. Strong understanding and practical knowledge of SFDA, GCC, and MENA regulatory frameworks and guidelines. Proficiency in Microsoft Office Suite and regulatory submission platforms. Personal Skills

Fluency in both English and Arabic (written and spoken) is essential. Seniority level

Mid-Senior level Employment type

Full-time Job function

Legal Industries

Pharmaceutical Manufacturing

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