About the role#
As a Regulatory Affairs intern, you will work within our medical equipment manufacturing operations. You will gain exposure to global regulatory strategy and compliance by working with teams such as R&D, Supplier Quality, Marketing, and Clinical Affairs. This role is a full-time, paid summer 2027 opportunity based in Portage, Michigan.
What you'll do#
- Monitor global regulatory changes by performing intelligence activities.
- Help prepare regulatory submissions to register products for international markets.
- Shadow Regulatory Affairs Specialists during new product development meetings.
- Assist with post-market regulatory reporting projects to monitor device performance.
- Contribute to the creation of regulatory assessments and change notification strategies.
What you'll need#
- Current enrollment in a Bachelor’s or Master’s degree program in Biomedical Engineering, Biology, Chemistry, or a related field.
- A cumulative GPA of 3.0 or higher.
- Proficiency in Microsoft Office including Excel, Word, and PowerPoint.
- Strong written and verbal communication skills.
- Legal authorization to work in the United States without sponsorship.
Location & details#
- This position is located on-site in Portage, Michigan.
- The internship takes place during the summer of 2027.
- This role is full-time.
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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