Regulatory & Technical (RegTech) Specialist

Regulatory & Technical (RegTech) Specialist – Dubai, UAE

M R G Pharmaceutical Consultancies L.L.C (Medical Regulations Gate – MRG)

Employment type:

2–4 years in regulatory affairs and registration (pharma and medical devices)

Medical 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.

We 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.

• Prepare, 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 registration
• Take part in MRG's regulatory digital transformation: help design, test and improve the platforms, tools and automated workflows we use to manage registrations
• Turn regulatory requirements and processes into structured data, templates and digital checklists
• Keep regulatory data in MRG's systems accurate and up to date, including submissions, licences, deadlines and client files
• Use digital tools and AI to speed up dossier preparation, gap checks and regulatory tracking
• Support the BD team with client meetings, technical presentations, proposals and regulatory pathway assessments
• Review client dossiers and technical documents for gaps and give clear regulatory advice
• Keep up with UAE regulatory and e-submission updates and share them with the team and clients
• Coordinate with MRG's regulatory and RegTech teams in KSA and Egypt on multi-market projects

• Bachelor's degree in Pharmacy
• Active UAE pharmacist licence (MOHAP, DHA or DOH)

– required

• 2–4 years of experience in regulatory affairs and product registration for pharmaceuticals and medical devices
• Working knowledge of UAE registration requirements for pharmaceuticals, medical devices or cosmetics
• Comfortable with digital tools and keen to use technology to improve regulatory work
• Excellent written and spoken English; Arabic is a plus
• Comfortable working in technical and client-facing roles
• Organised and detail-focused, and able to manage several files at once

Nice to Have

• Experience with GCC or SFDA submissions
• Hands-on use of regulatory information systems, e-submission portals, or tools such as Excel, Power BI, low-code platforms or AI assistants
• Exposure to business development or client account work
• Familiarity with ISO 13485 or quality systems

• A key role in a growing regional regulatory firm
• Exposure to multi-market projects across the GCC and the wider region
• Room to grow across regulatory affairs, regulatory technology and business development
• Competitive package based on experience

Send your CV and a copy of your UAE pharmacist licence through LinkedIn or to [[email protected]].

Please use the subject line: "RegTech Specialist – UAE".