bostonscientific-posted 10 days ago
$69,500 - $132,000/Yr
Full-time • Mid Level
Onsite • Maple Grove, MN
5,001-10,000 employees

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: Boston Scientific is looking for a highly motivated Process Engineer II 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. Work Mode: At Boston Scientific, we value collaboration and synergy. This role follows an onsite work model, requiring employees to be in our local office at five days per week. Relocation: Relocation assistance is not available for this position at this time. VISA: Boston Scientific will not offer sponsorship or take over sponsorship of an employment VISA for this position at this time.

  • Assesses process capabilities, prioritizes process improvement opportunities, and innovates and implements process improvements on multiple and moderately complex processes.
  • Applies technical knowledge to innovate, design, and develop processes, procedures, tooling and/or automation.
  • Executes the functional deliverables associated with the PDP/TDP, Project Management, and Quality Systems.
  • Prepares and presents technical data and recommendations at technical reviews.
  • Writes validation protocols and reports applicable to new processes.
  • Ensures proper documentation is completed to meet quality systems requirements. (e.g., BOM’s, Routers, FMEA’s, etc.)
  • Oversees development builds associated with the project using special work requests.
  • Develops qualified production lines.
  • Provides Design for Manufacturability (DFM) input to the engineering print package.
  • Contributes ideas to or generates Intellectual Property submissions.
  • Trains and/or provides work direction to technicians and may train manufacturing personnel when required as part of a validation.
  • May serve as core team member or extended team member on new product projects.
  • Bachelor’s degree in Engineering or related technical field
  • Minimum of 2 years of professional engineering experience relevant to this role
  • 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
  • Prior experience in medical device industry or similar highly-regulated industry
  • 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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