About the role#
This internship offers an opportunity to gain experience in global regulatory strategy and compliance within the medical technology field. You will work cross-functionally with teams including R&D, Supplier Quality, Marketing, and Clinical Affairs to ensure products meet regulatory requirements and reach patients safely.
What you'll do#
- Perform regulatory intelligence activities to monitor changes in global regulations.
- Assist with preparing regulatory submissions to register products internationally.
- Shadow RA Specialists during new product development meetings.
- Support post-market regulatory reporting projects to monitor device performance.
- Contribute to the development of regulatory assessments and change notification strategies.
What you'll need#
- Currently pursuing a Bachelor’s or Master’s degree in Biomedical Engineering, Biology, Chemistry, or Computer Engineering.
- Must remain enrolled in a degree-seeking program after the internship concludes.
- Cumulative GPA of 3.0 or higher.
- Proficiency in Microsoft Office, specifically Excel, Word, and PowerPoint.
- Must be legally authorized to work in the U.S. without sponsorship.
Location & details#
- Term: Summer 2027.
- Modality: Remote.
- Employment type: Full-time, paid internship.
About Stryker
Stryker is a medical equipment manufacturer based in Kalamazoo, Michigan. The company produces medical devices and surgical instruments for the MedSurg, Neurotechnology, and Orthopaedics sectors. It operates globally with over 53,000 employees and maintains more than 44 manufacturing and research facilities. Stryker reported 2024 sales of 22.6 billion dollars.
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