• Collaborate with product, development, and IT teams to understand complex hardware and software requirements • Design, develop, and execute detailed test plans, test cases, and test scripts for end-to-end solutions • Participate actively in Agile ceremonies to ensure quality is embedded throughout the development lifecycle • Perform in-depth functional, performance, reliability, and compatibility testing on various hardware asset management functions • Conduct rigorous functional, regression, integration, system, and user acceptance testing for software asset management functionality • Lead testing efforts specifically for ServiceNow's Software Asset Management and Hardware Asset Management modules • Utilize defect tracking tools to log, track, and manage issues • Generate comprehensive test reports

Title: Senior Quality System Engineer Location: Maple Grove, MN, United States Hybrid Job Description: 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: As a Senior Quality System Engineer supporting external audits, the incumbent will be a key Quality representative responsible for driving Audit Excellence at the Maple Grove and Arbor Lakes sites. The incumbent will lead and coordinate efforts around audit readiness, preparation, execution, and closure activities. This includes interfacing with regulatory authorities (e.g., FDA, Notified Bodies, and global agencies), site quality teams, and global stakeholders. This role will also contribute to internal audit execution and support Boston Scientific's participation in the FDA's 'Case for Quality' program. Work model, sponsorship, relocation: At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office Maple Grove, MN 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 Maple Grove external audit preparation, execution, and closure activities, including managing nonconformance and action response processes as needed. - Lead and support audit readiness strategies for both Maple Grove and Arbor Lakes sites. - Serve as the primary site representative on the External Audit Global Community of Practice. - Collaborate with other Boston Scientific sites to provide cross-site external audit support as needed. - Execute internal audits periodically for the Maple Grove and Arbor Lakes sites. - Support continued participation in the Medical Device Discovery Appraisal Program as part of FDA's 'Case for Quality.' - Promote a work environment that supports the Global Quality Policy, continuous improvement, and Boston Scientific's Core Values. - Serve as an effective leader or team member in support of quality disciplines, decisions, and practices. - Apply systematic problem-solving methodologies to identify, prioritize, communicate, and resolve quality issues. - Partner with internal teams to provide guidance on Boston Scientific's Quality Management System and applicable regulations/standards. Required qualifications: - Minimum of Bachelor's degree and 5 years' experience in the medical device or pharmaceutical industry. - Minimum of 2 years' experience in a Quality Systems role that includes internal or external audit support. - In-depth knowledge of regulations/standards such as 21 CFR 820 and ISO 13485. - Strong understanding of quality principles and interrelated job functions. - Highly detail-oriented with strong analytical skills. - Ability to make sound, risk-based decisions. Preferred qualifications: - Proven experience managing, coordinating, or supporting external audits of medical device quality systems. - Minimum of 5 years' experience in audit support (internal, supplier, notified body, or regulatory audits). - Excellent verbal and written communication, interpersonal, project management, and organizational skills. - Ability to understand procedural documents and evaluate documents for compliance with applicable regulations and requirements. - Ability to collaborate and communicate effectively across all levels of the organization. - Ability to be proactive, work independently, and contribute to a highly visible team. 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 www.bscbenefitsconnect.com-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. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above. Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements). Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements). For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability. As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn't just business, it's personal. And if you're a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you! At Boston Scientific, we recognize that nurturing a diverse and inclusive workplace helps us be more innovative and it is important in our work of advancing science for life and improving patient health. That is why we stand for inclusion, equality, and opportunity for all. By embracing the richness of our unique backgrounds and perspectives, we create a better, more rewarding place for our employees to work and reflect the patients, customers, and communities we serve. Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company's policies or protocols change with regard to COVID-19 vaccination. Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law. Nearest Major Market: Minneapolis Job Segment: Medical Device Engineer, Pharmaceutical, Compliance, Senior Quality Engineer, Internal Audit, Engineering, Science, Legal, Finance

• Lead the implementation and governance of the External Manufacturing Quality Management (EMQM) program at Kevin’s Natural Foods. • Ensure external manufacturers comply with Kevin’s and Mars Quality Management standards. • Own supplier qualification, approval, and ongoing performance management. • Act as a key technical authority ensuring quality and food safety standards across external partners. • Support both strategic (supplier development, program deployment) and tactical (audits, issue resolution) activities. • Define validation and verification programs to ensure product equivalency and food safety. • Drive visibility of external manufacturer quality performance and lead continuous improvement initiatives. • Manage change control processes impacting quality and food safety. • Facilitate supplier quality processes, policies, and onboarding frameworks. • Develop and improve RACIs and ways of working for material and supplier onboarding. • Monitor and improve inbound raw and packaging material quality across sites. • Establish KPIs and metrics to track supplier quality performance and compliance. • Conduct supplier audits (low, medium, high risk) to assess capability and compliance. • Lead initial supplier assessments and ongoing verification activities. • Identify gaps and drive corrective and preventative actions (CAPA) with suppliers. • Maintain supplier status, risk assessments (e.g., EMPRA), and technical documentation. • Partner with Procurement, R&D, and project teams to support external manufacturing in innovation projects. • Act as the quality lead for co-manufactured product development. • Ensure suppliers meet quality and food safety requirements for new product launches. • Lead investigations related to external manufacturing quality incidents. • Conduct risk assessments and determine product disposition. • Identify root causes and ensure effective CAPA implementation. • Monitor trends and incorporate learnings into continuous improvement efforts. • Drive supplier development initiatives to improve capability and performance. • Contribute quality insights to sourcing and supply strategies. • Engage with global and regional quality communities to align on best practices. • Support management reviews with data-driven recommendations. • Require regular interactions with external manufacturers, suppliers, and global quality teams. • Other duties as assigned or necessary.

• Perform manual testing of customer-facing web and mobile applications, focusing on usability, edge cases, and real-world user scenarios • Design, develop, and maintain automated test frameworks for web, mobile, and backend systems • Build and execute end-to-end, regression, and integration tests across customer-facing products • Validate backend services and RESTful APIs that support web and mobile experiences • Perform cross-browser and cross-device testing using tools such as BrowserStack • Collaborate with product managers and engineers to define test plans, acceptance criteria, and release readiness • Identify, document, and track defects, ensuring clear reproduction steps and timely resolution • Integrate automated tests into CI/CD pipelines • Continuously improve QA processes, tooling, and test coverage • Participate in release validation and post-release monitoring as needed