Summer 2027 Internship - RA/QA - Post Market Regulatory Affairs (Virtual)

About the role

Stryker is offering a virtual summer 2027 internship in Regulatory Affairs / Quality Assurance, focused on post-market regulatory affairs. The intern works cross-functionally with teams such as R&D, Supplier Quality, Marketing and Clinical Affairs, contributing to projects that ensure products meet regulatory requirements and reach patients safely and effectively. The internship is listed as onsite in the source but is advertised as virtual.

Key responsibilities

• Perform regulatory intelligence activities to monitor changes in global regulations and support strategy updates
• Assist with preparing regulatory submissions to register products internationally
• Shadow RA specialists during new product development meetings to understand the collaborative design and development process
• Support post-market regulatory reporting projects that monitor device performance and identify potential safety or quality issues
• Contribute to regulatory assessments and change notification strategies to minimize disruption to product registrations or approvals

Required profile

• Currently pursuing a Bachelor's or Master's degree in a scientific or technical discipline (Biomedical Engineering, Biological Sciences, Chemistry, Software Engineering or related fields) and must remain enrolled in a degree-seeking program after the internship
• Cumulative 3.0 GPA or above, verified at time of hire
• Legally authorized to work in the U.S. and does not require sponsorship now or in the future
• Strong written and verbal communication skills, with demonstrated leadership, problem-solving and organizational skills

Required skills

• Proficiency in Microsoft Office (Excel, Word, PowerPoint)
• Eagerness to learn in a dynamic environment

What we offer

• $20 minimum to $35 maximum hourly wage
• Sign-on bonus
• 11 paid holidays annually
• Paid corporate housing or a living stipend, depending on hiring location