Regulatory Affairs Intern
ResMed · Sao Paulo, Brazil
RegulatoryPart-timeCompany career page
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Role summary
ResMed seeks a regulatory affairs intern based in the São Paulo area to support the LATAM regional team with product submissions and regulatory compliance activities. The role involves collaborating across teams to obtain market access for medical devices and software while maintaining regulatory documentation and communications with stakeholders.
What they're looking for
- Currently enrolled in Bachelor's degree program in Life Sciences or Engineering; 3rd or 4th year preferred
- Fluent English communication skills; Portuguese as native language
- Proficient with Microsoft Office tools
- Detail-oriented, organized, and able to independently manage stakeholder follow-up
What you'll be doing
- Support preparation and compilation of premarket registration submission documents for Latin American markets
- Collaborate with regional RA, product development, clinical, marketing, and commercial teams on pipeline execution
- Track, maintain, and archive regulatory records and submission documentation
- Facilitate communications with internal stakeholders, health authorities, and regulatory consultants on submission status and strategy
- Assist with regulatory impact assessments for new or updated regulations and standards
Privacy & handoff
This role links to ResMed's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.