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# Design Quality Engineer I

- **Company:** Boston, Inc.
- **Location:** Marlborough, MA, United States
- **Experience:** Starter
- **Salary:** $62,800.0 - $119,300.0
- **Contract:** Franchise
- **Skills:** Minitab, Power BI, Statistics Packages
- **Published:** October 12, 2026
- **Apply:** https://diversityjobs.com/career/18629368/Design-Quality-Engineer-I-Massachusetts-Marlborough

## About the Role

* Minimum of a Bachelors degree in Biomedical Engineering, Mechanical Engineering, or related technical field.
 * Minimum of less than one year of experience.
 * Travel approximately 10%

Preferred Qualifications

 * Strong communication, collaboration, and documentation skills.
 * Internship, coop, or projectbased experience in engineering, quality, or medical devices.
 * Foundational understanding of design controls, risk management, and regulated product development.
 * Familiarity with basic statistical analysis tools; coursework in Minitab or PowerBI is a plus.
 * Exposure to problemsolving methodologies such as DMAIC, 5 Whys, or other rootcause tools.

## Description

The Design Quality Engineer I will be part of the Endoscopy Access and Patency franchise supporting sustaining for Self Expanding Stents (SES) manufactured at the Galway site. The Design Quality Engineer I will develop, establish and maintain quality engineering methodologies, systems, and practices which meet BSC, customer, and regulatory requirements. This engineer will serve as a Quality representative to improve awareness, visibility, communication on quality initiatives to support departmental, functional, site, divisional and corporate quality goals and priorities.

This position is part of the design site for the Endoscopy Division which supports New Product Development, Sustaining Engineering, and Life Cycle Management initiatives.

Work Mode:
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 three days per week., * Develop an understanding of Design Controls, Risk Management and Usability for Medical Devices

 * Provide quality and compliance input to cross-functional project teams, ensuring activities follow regulatory requirements and internal quality procedures.

 * Apply basic problem-solving tools (e.g., 5 Whys, Is/Is Not) with mentorship to support identifying, prioritizing, communicating, and resolving quality issues.
 * Contribute to ongoing improvements within quality and/or business processes by identifying opportunities to streamline documentation, processes, or tools.

 * Develop working relationships across departments and assist in communicating quality priorities and findings.
 * Support internal and external regulatory audits as required.

 * Provide quality and compliance input for post market product sustaining activities, such as design changes, supplier auditing and surveillance, design concessions, product CE marking and safety certification, customer complaint investigations, NCEP's, CAPA's and Field Signals.