Regulatory Affairs Specialist بدوام كامل في الإمارات العربية المتحدة
التخصص
متفرقات
نوع الدوام
دوام كامل
الخبرة
أي مستوى
الموقع
الإمارات العربية المتحدة
وصف الوظيفة
Location: Dubai, UAEEmployment Type: Full-timeIndustry: Pharmaceuticals / Medical Devices / Aesthetic HealthcareAbout the RoleWe are looking for a Regulatory Affairs Specialist to manage regulatory activities related to product registration, renewals, submissions and compliance with UAE health authority requirements.The ideal candidate will have previous Regulatory Affairs experience in the UAE, with experience handling regulatory requirements for medical devices, pharmaceutical, aesthetic or healthcare products preferred.Key ResponsibilitiesManage product registration and renewal processes with relevant UAE health authorities.Prepare, review, and submit regulatory documentation and applications.Maintain accurate regulatory records, certificates, registrations, and product documentation.Monitor registration and renewal timelines and ensure submissions are completed on schedule.Coordinate with UAE health authorities regarding regulatory submissions, queries, and required documentation.Review product documentation for completeness and regulatory compliance.Support regulatory submissions for new products, variations, renewals, and updates.Coordinate with internal teams, suppliers, and manufacturers to obtain required regulatory documents.Stay updated on applicable UAE regulatory requirements, guidelines, and procedures.Support the company in maintaining compliance with applicable regulatory requirements.Assist with regulatory audits, inspections, and authority correspondence when required.RequirementsPrevious experience in Regulatory Affairs within the UAE is required.Experience with UAE health authority registration and regulatory submissions.Experience in medical devices is preferred.Experience in pharmaceutical, aesthetic, healthcare, or related products is an advantage.Strong knowledge of regulatory documentation and submission processes.Good attention to detail and strong document management skills.Ability to coordinate effectively with health authorities, suppliers, manufacturers, and internal teams.Strong written and verbal communication skills.Ability to manage multiple registrations, renewals, and regulatory deadlines simultaneously.What We OfferA professional working environment within the healthcare and medical aesthetics industry.Exposure to regional regulatory and product registration activities.Opportunities to work with international healthcare and medical device products.Career growth within a growing organization.How to ApplyInterested candidates are invited to submit their CV through LinkedIn. Please highlight your UAE Regulatory Affairs experience and relevant product registration experience in your application.
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