Regulatory Associate

About Our Client:Our client is a global pharmaceutical leader with a strong presence in Dubai focused on delivering innovative medicines, vaccines and healthcare solutions. They are committed to improving patient outcomes, advancing research, and supporting regional health initiatives.Key Responsibilities:Prepare ready-to-submit regulatory dossiers including Labelling, CMC, administrative sections, renewals/annual reports and site registrations.Manage artworks using Vista and VistaVac tools.Update and monitor regulatory activities in databases such as Veeva Vault.Prepare administrative documents related to PoA and CPP.Ensure all documents are accurately translated in compliance with Health Authority requirements.Maintain regulatory compliance for products in line with country-specific requirements.Adhere to all internal and external requirements, procedures and tools.Collaborate with the company to maintain a safe and compliant workplace.Requirements:Bachelor's degree in Pharmacy, Medicine, Veterinary Science or preferably in Life Sciences.3‑4 years of experience in Regulatory Affairs or Quality Assurance with exposure to international or local regulatory environments.Proven project management experience within the pharmaceutical industry or a regulatory setting.Benefits:Employee Benefits as per the UAE Labour Law.#J-18808-Ljbffr