Senior Manufacturing Engineer
📋 Role Overview & Responsibilities
Work mode: OnsiteOnsite Location(s): Arden Hills, MN, US, 55112 Arden Hills, MN, US, 55112Additional Location(s): N/A
Diversity - 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. About the role:Our team in Arden Hills, MN is searching for a Senior Manufacturing Engineer to join their team. The Senior Manufacturing Engineer will lead continuous improvement initiatives, new product integration projects, and will provide daily support to the production floor to ensure that product, processes, material, and equipment meet the (Safety, Quality, Service, and Cost) business goals and objectives. He/she/they will routinely partner with cross-functional and cross-site teams (Production, Quality, Regulatory, R&D, Process Development, Supply Chain, etc.) to evaluate, troubleshoot and implement manufacturing processes within the business unit. Your responsibilities will include: Leads cross-functional project teams: Coordinates, manages, communicates, and documents project goals and progress. Supports technicians during troubleshooting activities when complex technical issues arise on the production floor. Identify, analyzes, and proposes process and product improvements making use of continuous improvement tools. Assesses the feasibility of new technologies, products, and equipment in the area. Designs and coordinates applicable engineering tests and experiments. Summarizes, analyzes, and draws conclusions from complex test results. Designs and prepares engineering reports and communicates results to the technical and leadership audiences. Completes and manages Capital Equipment Request Authorizations (CERA’s) Train team members, including engineers, technicians, and product builders on specific tasks. Participates in the development of junior staff by providing guidance and offering counsel. In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. Required qualifications: Bachelor’s degree in engineering 5+ years of experience (advanced degree with 3+ years of experience may be considered)Experience performing equipment validation and qualification activities Experience solving advanced technical problems Strong understanding of manufacturing problem solving/root cause analysis Experience utilizing data analytics to impact improvements in manufacturingPractical understanding of process improvement (DMAIC) and production flow (LEAN manufacturing) tools
Preferred qualifications: Medical device, or other regulated industry experience Experience managing and leading multiple projects simultaneously
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