Manufacturing Engineer II

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Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

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.

The role of a Manufacturing Engineer II is to execute engineering initiatives for the daily support of products, processes, materials, and equipment to meet operations goals (i.e., safety, quality, delivery, cost, and productivity). In a fast-paced and dynamic environment, this position will be responsible for supporting manufacturing lines in either the Endoscopy or Urology production unit. He/she/they will work cross‑functionally with quality, production, R&D, and project management teams to achieve goals, as well as update, improve, or add new manufacturing processes.

Boston Scientific was recently ranked as one of Forbes’ Best Employers for Engineers in America
—a testament to our investment in innovation, collaboration, and long‑term career growth for engineering professionals.

This role requires an onsite workmode from our Spencer, IN office. Relocation assistance is not available for this position and Boston Scientific will not offer sponsorship or take over sponsorship of an employment VISA for this position at this time.

• Monitor performance of equipment and processes, providing troubleshooting and root cause analysis of non‑conformances, low yields, or other quality/production issues.
• Communicate effectively to an audience consisting of peers, operations management, and supporting divisions (R&D, Sustaining Engineering, Project Management, etc).
• Plan, organize and prioritize daily work to meet production and project goals.
• Apply problem solving and process improvement methodologies to complex and diverse manufacturing processes, across multiple product lines—driving root cause analysis and resolution.
• Recognize quality signals and elevate appropriately within the quality system requirements.
• Support projects with cross‑functional team members working towards common business goals.
• Work collaboratively with divisional customer teams (R&D, Sustaining Engineering, Regulatory, Supply Chain, Quality, other) to deliver on new product introductions, change management, process improvements, or business continuity projects.
• Gather, analyze, and summarize data—drawing conclusions, and reporting out to peers and management.
• Takes initiative to identify improvement opportunities, prioritize them, communicate them to the appropriate levels and sees them through to completion.
• 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.

• Bachelor’s Degree in an Engineering discipline.
• 2+ years of manufacturing, process or related engineering experience.
• Strong bias for action and ability to effectively prioritize work and deliver business results in a fast-paced, constantly changing environment.
• Experience in manufacturing problem solving and process improvement tools such as DMAIC, as well as fundamentals of change management and equipment qualification.
• Strong verbal and written communication skills, including technical writing skills.
• Experience with Minitab or other data analysis, statistical & process improvement tools.

• Experience in medical device manufacturing technologies such as shape forming plastics, ultrasonic welding, adhesives, injection molding, laser marking, and sterile barrier sealing.
• Lean manufacturing experience.
• Experience working in PTC Windchill Product Lifecycle Management software or comparable platform.
• Basic knowledge of business intelligence software such as Power
  
  BI and Tableau.
• Basic knowledge of 3D…