Quality Intern

Boston Scientific•Arden Hills, MN

3d•$43,368 - $73,736•Onsite

About The Position

Boston Scientific is hiring a Quality Engineering Intern to support quality engineering and patient safety in a fast-paced, dynamic manufacturing environment. The Quality function develops, establishes, and maintains quality engineering methodologies, systems, and practices that meet company, customer, and regulatory requirements. The intern will represent Quality in initiatives supporting departmental, functional, site, divisional, and corporate goals and priorities, and will collaborate across functions to improve manufacturing processes. The position is on-site at the Boston Scientific Corporate location in Arden Hills, Minnesota, at least five days per week. Relocation and housing assistance may be available to eligible applicants. The internship must cover one of the stated program periods: May 17 through August 6, or May 24 through August 13. Applicants must be able to work in the United States without company sponsorship, now or in the future.

Requirements

Must graduate between Fall 2027 and Spring 2029.
Currently pursuing a bachelor's or graduate degree in Biomedical Engineering, Electrical Engineering, or Mechanical Engineering.
Must commit to one full internship period: May 17–August 6 or May 24–August 13.
Must be eligible to work in the U.S. without company sponsorship, now or in the future, for employment-based work authorization.
Must have reliable transportation to and from the Boston Scientific Corporate location in Arden Hills, Minnesota.
Proficiency with Microsoft Office tools, including Word, Excel, PowerPoint, and Outlook.

Nice To Haves

Clear written and verbal communication of complex data and processes.
Ability to work collaboratively with cross-functional teams.
Self-starter who can identify improvement opportunities and is eager to learn new technologies and develop new solutions.
Knowledge of analytical techniques and statistical analysis.
Previous internship or co-op experience supporting medical device development and manufacturing.
General knowledge of Power BI or similar data visualization tools.

Responsibilities

Act as an effective leader or team member in supporting quality disciplines, decisions, and practices.
Use systematic problem-solving methods to identify, prioritize, communicate, and resolve quality issues.
Apply technical knowledge to innovate, design, develop, and sustain processes, procedures, tooling, and equipment for medical devices.
Support the development and execution of streamlined business systems to identify and resolve quality issues.
Collaborate with a diverse cross-functional team and apply academic knowledge to real-world problems.
Contribute to value improvement projects, including yield improvements, process improvements, and materials cost savings.
Apply design-for-manufacturing principles to develop tooling and equipment for manufacturing lines for new products.
Create inspections or inspection systems to ensure products meet critical requirements.