Quality Engineer II

Skip to main contentDashboardProfileJoin Talent NetworkSign InEnglishSingle PositionView All JobsHybridQuality Engineer IIArden Hills US-MN, United States | N/A No longer accepting applications.Work ModeOnsiteRequisition ID613760Additional Location(s):  N/ADiversity - Innovation - Caring - Global Collaboration - Winning Spirit - High PerformanceAt 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.           Quality Engineer IIAbout the Role:At Boston Scientific, the Quality Engineer II will provide direct Quality Engineering support to ensure manufacturing and delivery of the highest quality product to our customers and patients.In a fast-paced and dynamic environment, the Quality Engineer II is responsible for manufacturing line processes, partnering cross-functionally with product and process development, manufacturing engineering, and production teams to achieve business unit goals. In this dynamic production environment, they have the opportunities to develop, establish and maintain quality engineering methodologies, systems, and practices. Serving as representatives of the Quality organization, they will improve awareness, visibility and communication on quality initiatives to support departmental, functional, site, divisional and corporate quality goals and priorities.Your Responsibilities Include:Partners with Manufacturing Engineering and Production core team members for daily manufacturing line support decisions and practices.Collaborates with cross-functional team to evaluate manufacturing results, assist defect detection, primary cause identification, and understanding corrective and preventative actions.Identifies and implements effective process control systems to support the development, qualification, validation and verification to meet or exceed internal, external, and regulatory requirements.Supports a culture of continuous improvement by advancing improvements to existing processes and controls.Proactively investigates, identifies, and implements best-in-class Quality Engineering practices.Applies sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.Broadly engages with production teams across all shifts to develop and support solutions to improve outgoing quality.Provide task direction, coaching, and mentorship for technician team members.Participate in team decision-making and display team problem-solving/communication skills.What We’re Looking For:Required Qualifications:Bachelor’s degree in engineering, technology, mathematics, or related science2+ years of relevant experience in a regulated industryStrong verbal and written communications skills; Good documentation practicesWorks effectively in a Controlled Environment Area (CEA) manufacturing environmentSelf-starter with a proven ability to successfully work with minimal supervisionKnowledge of basic Quality Management SystemsProficient with Microsoft Office tools (Word, Excel, PowerPoint, Outlook)Preferred Qualifications:Medical device experienceComfortable with utilizing analytical equipment (including microscopes)Strong analytical skills, problem solving, and statistical analysis (Excel, Minitab)Experience with the following disciplines: manufacturing/process engineering, post-market complaints, supplier quality, CAPA, risk managementExperience running/owning nonconforming event risk assessments and investigationsProficient using manufacturing control software (various MES, MasterControl, etc.)Project management experienceRequisition ID: 613760 Minimum Salary: $ 71500 Maximum Salary: $ 135800 The anticipated compensation listed above and the value of...