About the Role

We are looking for a motivated junior professional to support regulatory activities across multiple African and Middle Eastern markets. You will work with international manufacturers, digital health companies, and regional authorities to ensure medical devices and SaMD comply with local regulations.

Responsibilities

• Assist in preparing regulatory submissions (dossiers, registrations, renewals).

• Support conformity assessments and documentation reviews.

• Coordinate with health authorities and local partners.

• Contribute to post-market surveillance processes.

• Maintain regulatory databases and trackers.

• Prepare summaries, reports, and compliance updates.

Requirements

• Degree in a scientific, biomedical, pharmaceutical, or engineering field.

• Strong understanding (or willingness to learn) of medical device regulations.

• Excellent organization and communication skills.

• Ability to work remotely with international teams.

• Fluency in English (French or Arabic is a plus).

• Residence in one of the listed countries.

What We Offer

• Opportunity to grow within an expanding global medtech company.

• Real exposure to international regulatory strategies and digital health projects.

• Training in regulatory affairs, quality systems, and SaMD regulations.

• Flexible work environment and career development path.

→ Candidates should submit their CV and a short motivation message through the application form.