Senior Quality Supervisor

Senior Quality Supervisor

Work mode: Hybrid Onsite Location(s): Arden Hills, MN, US, 55112 Additional Location(s): US-MN-Arden Hills 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 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. At Boston Scientific, our work changes lives. As the Senior Quality Supervisor, Device Tracking, you will lead a high-performing team responsible for global medical device tracking operations and data management that help ensure patient safety, regulatory compliance and business continuity. In this highly visible leadership role, you will partner across Quality, Regulatory Affairs, IT, Operations, Distribution, Customer Service and Commercial teams to ensure the integrity of device tracking processes while driving continuous improvement and operational excellence.

Work model, sponsorship, relocation: At Boston Scientific, we value collaboration and synergy. This position is based in Arden Hills, Minnesota, and follows a hybrid work model requiring employees to be in our local office at least three 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:

• Lead, coach and develop a team of Business Process Administrators supporting global medical device tracking operations while fostering a culture of accountability, collaboration and continuous improvement.
• Drive the day-to-day execution of device tracking activities while ensuring compliance with FDA regulations, global quality system requirements and internal procedures.
• Oversee data quality, data integrity and records management within Global Medical Device Tracking (GMDT) and other enterprise systems.
• Lead continuous improvement initiatives, including process optimization, automation opportunities and system enhancements that improve operational performance.
• Partner with Regulatory Affairs and Product Teams to support new product introductions, acquisitions, regulatory commitments and device tracking assessments.
• Represent the Device Tracking function on cross-functional initiatives and evaluate the impact of business process and system changes.
• Monitor and improve operational performance using key performance indicators (KPIs), service-level agreements (SLAs) and quality metrics.
• Lead investigations into process issues and data discrepancies, implementing effective corrective and preventive actions (CAPAs) that reduce risk and improve performance.
• Support internal and external audits, regulatory inspections and quality management reviews.
• Build organizational capability through coaching, performance management, succession planning and employee development.
• Partner effectively across Quality, Regulatory Affairs, IT, Operations, Distribution, Customer Service and Commercial organizations to deliver business objectives.
• Demonstrate a commitment to patient safety and product quality by ensuring compliance with applicable regulatory requirements, Boston Scientific's Quality System and established quality processes.

Qualifications: Required qualifications: Associate degree in Business, Quality, Engineering, Life Sciences, Information Technology or a related field with a minimum of 7 years' relevant experience; or Bachelor's degree in Business, Quality, Engineering, Life Sciences, Information Technology or a related field with a minimum of 5 years' relevant experience. Minimum of 2 years' experience leading employees or cross-functional project teams. Working knowledge of FDA 21 CFR Part 821 and ISO 13485 requirements. Experience supporting quality systems, process controls, audits, CAPAs, change management or other compliance-related activities. Demonstrated ability to lead process improvements, manage operational metrics and drive execution of business objectives. Demonstrated analytical and problem-solving skills, with the ability to make sound decisions in a regulated environment. Demonstrated ability to communicate effectively and build strong partnerships across cross-functional teams and organizational levels. Preferred qualifications: Experience with medical device tracking, post-market surveillance, complaint handling or patient data management. Experience using GMDT (Global Medical Device Tracking), SAP, Salesforce, Jira or similar enterprise systems. Lean Six Sigma certification or demonstrated continuous improvement experience. Experience supporting acquisitions, system implementations or quality system integrations. Experience leading global teams or outsourced operations.

Requisition ID: 631461 Minimum Salary: $ 85000 Maximum Salary: $ 161500 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 and training, pertinent education including licensure and certifications, among other relevant business or organizational needs.