Boston Scientific-posted 27 days ago
$76,000 - $144,400/Yr
Full-time • Mid Level
Onsite • Maple Grove, MN
5,001-10,000 employees
Merchant Wholesalers, Durable Goods

This opportunity is focused on supporting clinical builds of a unique product, developing manufacturing technology for a commercial solution, and validating that process to support rapid growth in demand. Boston Scientific is looking for a highly motivated Process Engineer III to join our fast-growing team. In this role, you'll use your technical skills and passion for innovation to drive the commercialization of new products and improvements. You'll work hands-on to solve complex problems in a fast-paced, global environment, focusing on developing processes from concept to production. This position involves cross-functional collaboration to design and commercialize advanced technology, supporting process development across Boston Scientific's global plant network. At Boston Scientific, we value collaboration and synergy. This role follows a fully-onsite work model requiring employees to be in our local office five (5) days per week. Relocation assistance is not available for this position at this time. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.

  • Assess process capabilities, prioritize process improvement opportunities, and innovate and implement process improvements on multiple and moderately complex processes
  • Apply technical knowledge to innovate, design, and develop processes, procedures, tooling, and/or automation
  • Execute the functional deliverables associated with the PDP/TDP processes, Project Management, and Quality Systems
  • Write clean and concise work instructions that can be understood by product builders
  • Own/contribute to technical reports, validations, and qualifications by capturing experimental results
  • Complete proper documentation to meet quality systems requirements (e.g., BOM's, Routers, FMEA's, etc.)
  • Write validation protocols and reports applicable to new processes
  • Prepare and present technical data and recommendations at technical and business reviews
  • Oversee development builds associated with the project using special work requests
  • Provide Design for Manufacturability (DFM) input to the engineering print package
  • Partner cross-functionally to develop design specifications, test methods, and material selection
  • Contribute ideas to or generate Intellectual Property submissions
  • Train manufacturing personnel, when required, as part of early prototype line development and validation
  • May serve as core team member or extended team member on new product development projects
  • Bachelor's degree in Engineering or related technical field
  • Minimum of 3 years of professional engineering experience in ISO 13485 quality environment
  • Experience validating med device manufacturing processes
  • Hands-on mechanical aptitude
  • Demonstrated engineering fundamentals (LEAN , DFM, etc) and problem-solving skills
  • Demonstrated cross functional teamwork in a technically demanding environment
  • Strong written and verbal communication skills
  • Demonstrated use of Design for Six Sigma tools (Design of Experiments, problem solving)
  • Experience in New Product Development
  • Experience developing and characterizing various types of processes
  • Demonstrated understanding and usage of statistics to drive improvements; proficiency in Minitab
  • Demonstrated ability to develop equipment/fixtures/tooling from concept to production
  • Troubleshooting in combination with product yield and performance
  • Experience with mechanical design
  • Ability to schedule out timelines with specific milestones to achieve and demonstrated success
  • Open to travel (domestic or international) up to 10% of time
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