Process Engineer II - WATCHMAN

bostonscientificMaple Grove, MN
1d$69,500 - $132,000Onsite

About The Position

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 development and 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. This is a key opportunity in Process Development (PD) for WATCHMAN within Boston Scientific's Cardiology division. WATCHMAN continues to be an exciting growth driver for Boston Scientific. Boston Scientific ranked #2 among medical device companies on Forbes America's Best Places to Work for Engineers 2026 . Whether your passion lies in systems, software, human factors, or beyond, this is a place where you can grow your career and be part of something bigger—advancing science for life. At Boston Scientific, we value collaboration and synergy. This role follows an onsite work model requiring employees to be in our local office five (5) days/week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.

Requirements

  • Bachelor's Degree in Engineering or related technical field
  • Minimum of 2 years of professional engineering experience relevant to this role
  • Prior experience working in a team environment across functions and sites
  • Demonstrated engineering fundamentals (LEAN , DFM, etc), statistics, and problem-solving skills
  • Hands-on mechanical aptitude
  • Strong written and verbal communication skills

Nice To Haves

  • Fixture and equipment design or trouble shooting experience (CAD experience not required)
  • 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
  • Cardiology related experience
  • Medical device experience
  • Demonstrated cross-functional teamwork in technical environment
  • Demonstrated understanding and usage of statistics to drive improvements
  • Demonstrated problem solving skills
  • Development of new technology and early concept product & process generation
  • Ability to schedule out timelines with specific milestones to achieve and demonstrated success
  • Ability to travel up to 10% of the time
  • Boston Scientific experience

Responsibilities

  • Collaborate with R&D to develop product concepts, influence design specifications, and provide Design for Manufacturability (DFM) input
  • Work cross functionally to develop and deliver capable processes and equipment to operations
  • Apply technical knowledge to innovate, design, and develop processes, procedures, tooling, and/or automation
  • Assess process capabilities, prioritize process improvement opportunities, and innovate and implement process improvements on platform or derivative projects
  • Execute the functional deliverables associated with the PDP/TDP, Project Management, and Quality Systems
  • Gather, provide, and present technical data for technical reviews and decision making
  • Write work instructions, 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 and review validation protocols and reports applicable to new and updated processes
  • Oversee development builds associated with the project using special work requests
  • Contribute ideas to or generate Intellectual Property submissions
  • Train and/or provide work direction to technicians and engineers and may train manufacturing personnel when required as part of prototype line development and validation
  • May serve as a workstream lead or extended team member on new product development projects
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