Summer 2027 Internship - RA/QA - Post Market Regulatory Affairs - Virtual
Core
Summer intern in Post Market Regulatory Affairs 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 safety reporting for medical devices
Domain
Medical Devices / Healthcare Regulatory
Required skills
Regulatory intelligence, regulatory submissions, post-market reporting, change management, cross-functional collaboration, Microsoft Office proficiency
Preferred skills
Scientific or technical background (Biomedical Engineering, Biological Sciences, Chemistry, Software Engineering), leadership, problem-solving
Responsibilities
Monitor global regulations and support strategy updates, assist with international product registration submissions, shadow RA Specialists in new product development, support post-market regulatory reporting, contribute to regulatory assessments and change notification strategies
Seniority
Intern
