Summer 2027 Internship - RA/QA - Regulatory Affairs - Michigan
Core
Regulatory Affairs intern supporting global regulatory strategy, compliance, and product registration for medical devices.
Role type
Summer Regulatory Affairs Intern
Builds
Regulatory submissions, change notification strategies, and post-market safety reports for medical devices.
Domain
Medical Devices / Healthcare Regulatory Affairs
Deliverable
client delivery
Required skills
Regulatory intelligence, regulatory submission preparation, cross-functional collaboration, process documentation, strategic thinking
Preferred skills
Scientific or technical background (Biomedical Engineering, Biological Sciences, Chemistry)
Technologies
Microsoft Office (Excel, Word, PowerPoint)
Responsibilities
Monitor global regulatory changes, assist with international product registration submissions, support post-market regulatory reporting, contribute to regulatory assessments and change notification strategies.
Seniority
Intern