Regulatory Affairs Intern

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.