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 Intern, Regulatory Affairs
Builds
Regulatory submissions, change notification strategies, and post-market regulatory reports for medical devices.
Domain
Medical Devices / Healthcare Regulatory Affairs
Required skills
Regulatory intelligence, regulatory submissions, post-market reporting, change management, Microsoft Office proficiency
Responsibilities
Monitor global regulations and support strategy updates; Assist with preparing regulatory submissions for international product registration; Shadow RA Specialists during new product development meetings; Support post-market regulatory reporting projects; Contribute to regulatory assessments and change notification strategies.