About the role#
As a Regulatory Affairs intern, you will gain exposure to global regulatory strategy and compliance. You will work cross-functionally with teams including R&D, Supplier Quality, Marketing, and Clinical Affairs to ensure our 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 to observe the design process.
- 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, Chemistry, or a related field.
- Must remain enrolled in a degree-seeking program after the internship concludes.
- A cumulative GPA of 3.0 or above.
- Strong written and verbal communication skills.
- Proficiency in Microsoft Office, including Excel, Word, and PowerPoint.
- Legal authorization to work in the United States without the need for sponsorship.
Location & details#
- Location: Fremont, California.
- Term: Summer 2027.
- Modality: On-site.
- This is a 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.
How to get in at Stryker
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