{"id":1646481,"url":"https://alion.io/job/boston-scientific-supplier-quality-engineer-iii","title":"Supplier Quality Engineer III","company":{"id":1758528,"name":"Boston Scientific","domain":"bostonscientific.com","url":"https://alion.io/company/bostonscientific-com","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Eightfold","truth_index":{"grade":"B","score":82,"open_postings":72,"ghost_share":0.014,"stale_share":0.667,"repost_share":0.042,"time_to_fill_p50_days":32,"computed_at":"2026-10-29T05:49:05Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"middle","employment_type":null,"work_mode":"hybrid","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Arden Hills, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":78300,"max":null,"currency":"USD","period":"year","gross":null,"usd_annual":78300},"salary_estimate":null,"experience_years_min":5,"visa_sponsorship":true,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CAPA","optional":false},{"name":"Design Controls","optional":false},{"name":"ISO 13485","optional":true}],"status":"live","first_seen_at":"2026-03-06T20:52:09Z","employer_posted_date":"2026-10-01","last_verified_at":"2026-10-29T13:10:05Z","board_verified":true,"closed_at":null,"days_open":236,"trust":{"level":"stale","repost_count":0,"flags":["stale"],"days_open":236},"description":"Additional Location(s): N/A\nDiversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance\nAt 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.\nSUPPLIER QUALITY ENGINEER III - Electrophysiology External Operations\nThe External Operations organization focuses on Sourced Finished Medical Device (SFMD) at Boston Scientific and is a global, passionate team that oversees a diverse network of suppliers which manufacture finished devices for BSC distribution. The Supplier Quality Engineer III will demonstrate a primary commitment to patient safety and compliance through collaboration with cross-functional internal/external resources to continually improve our supplier’s manufacturing processes to ensure finished device quality. In this role, you will support SFMD products within the Electrophysiology division with a primary focus on Single-Use Devices and Capital Equipment.\nAdditionally, the Supplier Quality Engineer will support global sourcing, supplier manufacturing operations, and global quality systems by participating in global communities of practice and value improvement projects.\nWork model, sponsorship, relocation:\nAt 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. 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.\nFunction or Divisional Overview\nAt Boston Scientific, our products and technologies support the diagnosis and treatment of a wide range of medical conditions, with a focus on advancing less invasive care. Within the Electrophysiology (EP) portfolio, Boston Scientific develops, manufactures, and markets solutions designed to treat complex cardiac arrhythmias and enable precise, catheter-based interventions.\nThe EP portfolio includes technologies for cardiac mapping and navigation, radiofrequency ablation, diagnostic electrophysiology, EP recording systems, and intracardiac access and steerable sheath solutions, supporting physicians across the full EP procedure workflow. These products are designed to improve procedural efficiency, precision, and patient outcomes in the treatment of cardiac rhythm disorders.\nBoston Scientific continues to invest in innovation, clinical research, and global expansion within Electrophysiology, extending access to advanced therapies across key geographies. Through ongoing portfolio development and clinical evidence generation, the EP division supports the evolution of catheter-based treatment strategies for some of the most complex and prevalent cardiac arrhythmias.\nKey Responsibilities will inlcude:\nNew Product Development:\nCore team member to support product launch through execution of SFMD Plan deliverables for integration and/or onboarding of supplier and related products into BSC’s Quality System.\nLead the execution of SFMD quality deliverables and collaborate with cross-functional new product development teams to onboard finished medical device suppliers.\nGenerate and review quality plans, agreements, product specifications, component qualifications, design verification/validations, process validations, and incoming inspection requirements.\nLead and support initial on-boarding assessments, new manufacturing locations and supplier’s approved status\nSustaining Supplier Quality & Compliance\nResponsible for ongoing supplier qualification and performance monitoring based on supplier risk. Assess suppliers for technical, quality and manufacturing capabilities\nPlans and leads supplier audits to assess compliance with regulatory standards and Boston Scientific requirements, including audit scheduling investigation, and evaluation of audit observation and findings, reporting, follow-up, and confirmation of follow-up actions\nAssess & drive reactive as well as proactive supplier project(s)/investigations partnering with Supplier Engineering, Commercial Sourcing, Design Assurance.\nInvestigates & solves non-conformances due to product realization, product performance, incoming inspection, audit findings, & field failures related to supplier materials. Develop corrective action plan where necessary. Applies sound, systematic problem-solving methodologies in identifying, prioritizing, and resolving quality issues. Reviews and approves supplier corrective action plans and verification of effectiveness documentation\nSupports supplier change impact assessments, process change impacts, and design change implementations for suppliers within the BSC quality system requirements as well as supporting any requirements from the supplier’s Quality system.\nQuality record ownership requiring technical writing skillset to formally document investigations, testing and verification of effectiveness actions utilizing statistical and industry standard quality tools\nQuality System Champion:\nSupports Material Controls external regulatory body audits requests as required.\nLeads or supports Material Controls internal audit efforts.\nCollaborates with corporate and regional supplier quality organizations on policy, procedure, and guideline development. Includes generation, review, and implementation of these documents.\nIdentifies and advises management on potential improvements to quality systems and processes in the company.\nChampions 100% compliance to company policies and SOP’s.\nRequired Qualifications:\nMinimums of BS degree in engineering or technical field \nMinimum of 5 years of relevant experience.\nExperience in medical device, automotive, aeronautical, semiconductor, or other regulated industry.\nProject management: ability to influence cross functional global teams spanning Quality, Operations, R&D, and Sourcing.\nExperience in process validation, design controls, risk management, CAPA, SCAR.\nDomestic and international travel up to 25%. \nPreferred Qualifications:\n3+ years of medical device engineering experience preferred.\nProblem Solving and Project Management experience\nLeadership experience on a materials or service commodity team.\nLead auditor of quality systems experience (ISO 13485 or similar).\nASQ certification (CQE, , SSGB, SSBB) desired\nAbility to work independently; organized and self-driven.\nArticulate communicator; adept at packaging and appropriately scaling information to the intended audience.\nAbility to rapidly learn and use new software applications (e.g., PLM, ERP).\n\nRequisition ID: 625835\nMinimum Salary: $ 78300\nMaximum Salary: $ 148800\nThe 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.\nCompensation 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).\nCompensation 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).\nFor MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.\nBoston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn.\nBoston 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.\nPlease 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.\nAmong 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. 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