Design Quality Assurance Engineering Fall Co-op

Boston Scientific
$44,616 - $60,216Hybrid

About The Position

At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model, requiring employees to be in our local office at least four days per week. Relocation assistance may be available to those who meet the eligibility criteria. Boston Scientific will not offer sponsorship or take over sponsorship of an employment VISA for this position at this time We will consider qualified applicants of all ages who are starting (or restarting) their careers Our Purpose: As a Design Quality Assurance Engineering Fall Co-op will support Boston Scientific’s mission to serve more patients by improving product experiences across four key objectives: culture, agility, performance and compliance. You 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.
  • Work completed in this role directly supports clinical effectiveness by helping ensure high‑quality medical devices reach the people who need them.
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