About the role#
As a Regulatory Affairs Intern, you will support the commercialization of medical devices by maintaining global regulatory requirements and documentation. You will work within the Urology business, contributing to a robust product pipeline that supports treatments for kidney stone removal, prostate health, and urinary continence. This position offers exposure to global regulatory submissions and continuous improvement activities in a hybrid work environment.
What you'll do#
- Learn regulatory requirements necessary to commercialize medical devices.
- Support updates to EU MDR Technical Documentation.
- Prepare and submit regulatory submissions, such as FDA PMA supplements for manufacturing changes.
- Use regulatory advocacy to influence the regulatory process.
- Collaborate with cross-functional partners to support product and manufacturing changes, including drafting assessments regarding compliance with applicable regulations.
What you'll need#
- Current enrollment in a degree program with a graduation date between Fall 2026 and Spring 2027.
- Pursuing a degree in Biology, Biomedical Engineering, Public Health, Psychology, Communications, or other relevant fields such as Science, Healthcare, Engineering, Exercise Science, Math, Business, English, or a Master’s degree in Regulatory or Clinical Affairs.
- Proficiency in Microsoft Office Suite: PowerPoint, Word, Excel, and Outlook.
- Ability to commit to one of the following full-time internship periods: May 18th – August 7th OR May 26th – August 14th.
Location & details#
- This is a full-time, paid internship.
- The role is based in Minnetonka, MN, and Maple Grove, MN, requiring reliable transportation to both locations.
- This position follows a hybrid work model, requiring presence in the office at least three to four days per week.
- Please note that Boston Scientific will not offer visa sponsorship for this position.
