Design Quality Engineer

Diversity
- Innovation
- Caring
- Global Collaboration
- Winning Spirit
- High Performance

At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions.

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.

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.

Relocation assistance is not available for this position at this time.

Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.

• 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.

• 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%

• Strong communication, collaboration, and documentation skills.
• Internship, co-op, or project-based 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 problem-solving methodologies such as DMAIC, 5 Whys, or other root-cause tools.

Requisition

Minimum Salary:$62800

Maximum Salary: $119300

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see  will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience…