Muhrat Al Marasim
Talent & Professional Careers

Careers at Muhrat Al Marasim.

بوابة التوظيف واستقطاب الكفاءات التنظيمية

Join the Kingdom's elite healthcare regulatory team. Shape the future of medical technology, digital health, and pharmaceutical market access across Saudi Arabia.

Showing 4 open executive & scientific positions in Riyadh
Medical Devices & DiagnosticsFull-Time

Senior Regulatory Affairs Manager – MedTech & IVDs

Riyadh, Saudi Arabia (Hybrid) Full Time

Lead complex Class IIb and Class III SFDA MDMA submissions, mentor regulatory associates, and liaise directly with SFDA ...

Quality Assurance & OperationsFull-Time

Lead QMS & Compliance Auditor (ISO 13485 / GDP)

Jeddah, Saudi Arabia Full Time

Perform comprehensive QMS design, mock audits, and warehouse licensing (MDEL) preparation for multinational medical dist...

Pharma & BioTechFull-Time

Pharmaceutical Regulatory Affairs Specialist (eCTD)

Riyadh / Dubai Full Time

Manage GCC Centralized and SFDA national pharmaceutical eCTD dossiers (Modules 1-5), variations, and GMP site inspection...

Clinical & VigilanceFull-Time

Post-Market Vigilance & Safety Officer

Riyadh, Saudi Arabia Full Time

Coordinate 24/7 adverse incident reporting, manage SFDA Saudi Vigilance system notifications, and coordinate recall acti...

Medical Devices & DiagnosticsRiyadh, Saudi Arabia (Hybrid)

Senior Regulatory Affairs Manager – MedTech & IVDs

Lead complex Class IIb and Class III SFDA MDMA submissions, mentor regulatory associates, and liaise directly with SFDA scientific committees.

Candidate Prerequisites:
Bachelor's or Master's degree in Biomedical Engineering, Pharmacy, or Life Sciences.
Minimum 5 years of direct experience with SFDA GHAD portal submissions and technical file authoring.
In-depth knowledge of ISO 13485:2016, ISO 14971:2019, and EU MDR/IVDR.
Bilingual fluency in Arabic and English.