Quality Engineer III

Additional Location(s):   N/A 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.              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. The Quality Engineer III provides focused quality engineering support within the Urology RCPH manufacturing core team in Spencer, Indiana. This role develops, establishes and maintains quality engineering methodologies, systems and practices that meet Boston Scientific, customer and regulatory requirements. Serving as a quality representative, this role improves awareness, visibility and communication of quality initiatives while supporting departmental, functional, site, divisional and corporate quality goals and priorities. The Quality Engineer partners across manufacturing, engineering, product, supplier and divisional teams to advance patient safety, product quality, operational excellence and continuous improvement.   Work model, sponsorship, relocation: This is an on-site role based in Spencer, Indiana. Relocation assistance is not available for this position at this time.   Your responsibilities will include: • Provide focused quality engineering support for manufacturing operations and system/service support for Spencer RCPH (Retrievals, Catheters, Pelvic Health), partnering with Urology, PI IO&E, Endoscopy, CRM Cardiac and other Boston Scientific sites and divisions. • Provide manufacturing line support and monitor product quality to ensure compliance with established requirements. • Identify nonconformance events and initiate, own and complete NCEP records. • Determine and execute appropriate product and process containment associated with NCEP events. • Escalate CAPAs when appropriate and own and complete CAPA records. • Determine the scope of product impact during PIR ET, PIR and field action scenarios. • Partner with manufacturing engineers and product supervisors to provide leadership within the manufacturing core team. • Drive lean production and system processes and deliver measurable value through the VIP system. • Advance Protect the Core, Guardian and Delivering Excellence strategic goals, including complaint reduction, Quality Catch mitigations, workstation vulnerability score reduction, IPM improvement and preventive CAPAs. • Partner with cross-functional core team members and share ownership of deliverables related to PCA, new products, acquisition products, DCA product support, supplier engineering and supplier quality. • Collaborate with divisional Design Quality and R&D partners, serving as an internal voice of the customer across Urology, PI IO&E, Endoscopy, CRM Cardiac and other Boston Scientific sites and divisions. • Champion departmental and cross-functional engineering initiatives and serve as an effective leader or team member in supporting quality disciplines, decisions and practices. • Provide project direction, coaching and mentoring to engineering and technical team personnel. • Proactively investigate, identify and implement best-in-class quality engineering practices. • Apply systematic problem-solving methodologies to identify, prioritize, communicate and resolve quality issues, including associated risk documentation. • Review and