We are seeking motivated and a curious Summer Intern to join our team and support high-impact projects in Quality Assurance/Regulatory Affairs (QA/RA).

This internship provides hands-on experience working on meaningful, project-based assignments that directly support business priorities. Interns will collaborate with cross-functional teams, gain exposure to the medical device industry, and develop practical skills in their area of interest.

As part of the program, interns will participate in a signature initiative, the Intern Impact Project. Working as a cohort, interns will identify an opportunity to improve a process, experience, or area of the business, develop a solution, and present their recommendation to management at the conclusion of the internship.

Department Examples (Project-Based Work May Include)

QA/RA

• Support documentation related to quality systems, CAPA, or regulatory processes
• Assist with organizing and maintaining compliance-related records

• Support department-specific projects aligned with business needs and priorities
• Conduct research, analysis, and documentation to support team initiatives
• Assist in organizing, improving, or building processes and resources
• Collaborate with cross-functional teams to gather information and drive project progress
• Participate in team meetings, check-ins, and company-wide sessions
• Partner with fellow interns on the Intern Impact Project, including identifying opportunities, developing solutions, and preparing final recommendations
• Present project outcomes and Intern Impact Project recommendations to management at the conclusion of the internship Perform other duties as needed

Qualifications

• Currently enrolled in a college or university (or recent graduate)
• Interest in: QA/RA
• Strong organizational skills and attention to detail
• Effective communication and ability to collaborate across teams
• Ability to manage tasks, meet deadlines, and take initiative
• Proficiency in Microsoft Office (Excel, PowerPoint, Word) preferred