Regulatory & Technical (RegTech) Specialist

Regulatory & Technical (RegTech) Specialist – Dubai, UAECompany: M R G Pharmaceutical Consultancies L.L.C (Medical Regulations Gate – MRG) Location: Dubai, UAE (on-site) Employment type: Full-time Experience: 2–4 years in regulatory affairs and registration (pharma and medical devices)About MRGMedical Regulations Gate (MRG) is a licensed Authorized Representative and regulatory consultancy serving manufacturers of pharmaceuticals, medical devices and cosmetics across Saudi Arabia, the UAE, Egypt and Syria. We are ISO 13485:2016 certified and hold the AR licence directly, so our clients get one accountable partner from submission to market access.The RoleWe are growing our UAE office and are looking for a licensed pharmacist to join us as a Regulatory & Technical (RegTech) Specialist. The role combines three areas: UAE product registration, technical support to our Business Development team, and helping build MRG's digital regulatory platform. It suits someone who wants a regulatory career where regulation meets technology.Key ResponsibilitiesPrepare, compile and submit registration files for pharmaceuticals, medical devices and cosmetics with UAE authorities (MOHAP / EDE and relevant emirate-level regulators)Follow up on submissions, respond to authority queries and track approvals through to registrationTake part in MRG's regulatory digital transformation: help design, test and improve the platforms, tools and automated workflows we use to manage registrationsTurn regulatory requirements and processes into structured data, templates and digital checklistsKeep regulatory data in MRG's systems accurate and up to date, including submissions, licences, deadlines and client filesUse digital tools and AI to speed up dossier preparation, gap checks and regulatory trackingSupport the BD team with client meetings, technical presentations, proposals and regulatory pathway assessmentsReview client dossiers and technical documents for gaps and give clear regulatory adviceKeep up with UAE regulatory and e-submission updates and share them with the team and clientsCoordinate with MRG's regulatory and RegTech teams in KSA and Egypt on multi-market projectsRequirementsBachelor's degree in PharmacyActive UAE pharmacist licence (MOHAP, DHA or DOH) – required2–4 years of experience in regulatory affairs and product registration for pharmaceuticals and medical devicesWorking knowledge of UAE registration requirements for pharmaceuticals, medical devices or cosmeticsComfortable with digital tools and keen to use technology to improve regulatory workExcellent written and spoken English; Arabic is a plusComfortable working in technical and client-facing rolesOrganised and detail-focused, and able to manage several files at onceNice to HaveExperience with GCC or SFDA submissionsHands-on use of regulatory information systems, e-submission portals, or tools such as Excel, Power BI, low-code platforms or AI assistantsExposure to business development or client account workFamiliarity with ISO 13485 or quality systemsWhat We OfferA key role in a growing regional regulatory firmExposure to multi-market projects across the GCC and the wider regionRoom to grow across regulatory affairs, regulatory technology and business developmentCompetitive package based on experienceHow to ApplySend your CV and a copy of your UAE pharmacist licence through LinkedIn or to [jobs@mrg.com.sa]. Please use the subject line: "RegTech Specialist – UAE".