We are seeking a detail-oriented and proactive Regulatory Affairs Coordinator to support regulatory activities at our UAE-based manufacturing facility. This role is responsible for compiling and coordinating product and site-specific regulatory dossiers for submission to global health authorities including support for GMP audits. The ideal candidate will collaborate closely with Quality Assurance (QA) manufacturing and technical teams at the site as well as regional regulatory teams. Experience with local UAE and GCC regulatory requirements is preferred with an understanding of global CTD requirements.

• Collate compile and review regulatory dossiers for product and site registrations in various international markets including GMP audit dossiers.
• Ensure accuracy completeness and regulatory compliance of all documentation submitted.
• Review and verify the correctness and regulatory alignment of Artwork (AW) prior to submission. <...