Design Quality Assurance Engineering Fall Co-op
About The Position
This role supports Boston Scientific’s mission to serve more patients by improving product experiences across four key objectives: culture, agility, performance and compliance. The Design Quality Assurance Engineering Co-op will help develop, establish and maintain quality engineering methodologies, systems and practices that meet Boston Scientific, customer and regulatory requirements. This role serves as a quality representative, increasing awareness, visibility and communication of quality initiatives while supporting departmental, site and corporate goals. The co-op will provide hands-on design-quality assurance engineering support across new product development, sustaining engineering, and system- or service-related activities, contributing to the delivery of safe, effective, and high-quality medical technologies.
Requirements
- Currently pursuing a bachelor’s or graduate-level degree in Mechanical Engineering, Biomedical Engineering, or Industrial Engineering.
- Knowledge of data analysis and interpretation tools.
- Must graduate between Fall 2026 – Spring 2028.
- Must be eligible to work in the U.S. without company sponsorship, now or in the future, for employment-based work authorization.
- Must be able to commit to program dates July 13th - December 18th, 2026.
- Must have reliable transportation to and from the Marlborough, Massachusetts, Boston Scientific location; transportation will not be provided by the company.
Nice To Haves
- Desire to work in fast paced Cross-Functional Teams to maintain and support quality-engineering methodologies, systems, and practices that meet internal and external requirements.
- Interest in obtaining a job within the medical device industry upon graduation, preferably an interest in a quality role.
- Effective written and verbal communication skills for documenting work and collaborating with cross‑functional team members.
- Coursework or basic understanding of quality systems, design controls, risk management, or statistics (through classes, projects, or labs).
- Proficiency with Microsoft Office tools (Excel, Word, PowerPoint); experience with technical documentation is a plus.
Responsibilities
- Collaborate with Design Quality Assurance engineers on day‑to‑day efforts by supporting problem‑solving activities and gaining exposure to structured, systematic approaches for addressing quality initiatives.
- Act as an effective leader or team member in supporting quality disciplines, decisions, and practices while learning how quality analyses are performed in practice.
- Support quality efforts by assisting with the review and maintenance of design documentation by checking accuracy, organization, and traceability in accordance with established procedures.
- Gain hands‑on exposure to design control and quality system processes by working within a regulated medical device environment and following formal quality procedures.
- Assist with continuous improvement efforts by supporting the development and execution of business processes that help identify, communicate, and implement best-in-class practices for quality engineering systems.
- Support investigation activities by assisting with data gathering, documentation review, and problem‑solving exercises that help drive quality decisions.
- Contribute to the continuous improvement and sustainment of key Boston Scientific products through quality and documentation support activities.
Benefits
- Relocation assistance may be available to those who meet the eligibility criteria.
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What This Job Offers
Career Level
Intern
