Regulatory Affairs Intern
Core
Support the LATAM Regional Regulatory Affairs team with routine product submissions to obtain regulatory market access for innovative medical and non-medical software systems across Latin America.
Role type
Regulatory Affairs Intern
Builds
Regulatory submissions for medical devices and software as a medical device in Latin America
Domain
Medical Devices / Software as a Medical Device / Regulatory Compliance
Required skills
Technical writing, regulatory documentation preparation, stakeholder communication, record management, impact assessment tracking
Preferred skills
Knowledge of LATAM country-specific regulations, familiarity with global registration processes
Technologies
Microsoft Office
Responsibilities
Prepare and compile submission documents for premarket registrations; maintain general regulatory records and archive documentation; communicate with internal stakeholders, external health authorities, and regulatory consultants; track impact assessments on new regulations
Seniority
Intern
