Quality Engineer III

Quality Engineer III

Work mode:
Onsite Onsite Location(s):
Maple Grove, MN, US, 55311 Additional Location(s): US-MN-Maple Grove 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.

About the role:

Boston Scientific was recognized by Forbes as one of the Best Workplaces for Engineers in 2026, reflecting a culture where engineers do meaningful work. Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day. Join the Metals Core Technology (MCT) Quality team in Maple Grove, Minnesota, to improve patients' lives and make a meaningful impact on those around you.

In this dynamic production environment, you will have the technical autonomy to drive innovation, strengthen manufacturing processes and help transform customer experiences globally. In this role, you will collaborate with manufacturing engineers on line support activities and partner with product development teams to help ensure the development of robust new products. The incumbent will oversee multiple manufacturing processes on the production line and work cross-functionally with manufacturing engineering and production teams to achieve business unit objectives while providing quality leadership to the team.

Work model, sponsorship, relocation:
At Boston Scientific, we value collaboration and synergy. This is an on-site role requiring employees to work at our Maple Grove, Minnesota, location five days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is not available for this position at this time. Your responsibilities will include:
Identify and implement effective process control systems to support the development, qualification and ongoing manufacturing of products that meet or exceed internal and external requirements. Support a culture of continuous improvement by driving enhancements to existing process controls. Proactively investigate, identify and implement best-in-class quality engineering practices. Promote quality assurance, process controls and corrective and preventive action (CAPA) systems designed to meet or exceed internal and external requirements.

Apply sound, systematic problem-solving methodologies to identify, prioritize, communicate and resolve quality issues. Actively engage with production teams across all four shifts to develop solutions that improve outgoing quality. Provide input on and implement departmental and cross-functional engineering initiatives. Provide project direction, coaching and mentoring to technician team personnel. Perform process validation and verification activities and review related documentation.

Required qualifications:

Bachelor's degree in engineering, science or a related field. Minimum of 3 years' experience in a relevant field, including experience with process validation and verification activities and risk management documentation, such as design failure mode and effects analyses (DFMEAs) and process failure mode and effects analyses (PFMEAs). Strong data analysis skills using tools such as Excel and Minitab. Proven ability to work successfully with minimal supervision and take initiative.

Ability to manage multiple priorities and meet deadlines while maintaining strong attention to detail.

Preferred qualifications:

Experience owning nonconformance investigations, process improvement initiatives and corrective action projects. Experience leading cross-functional teams and driving projects to completion. Experience in the medical device industry or another highly regulated industry. Experience providing quality line support. Experience working in a manufacturing environment.