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Engineer II, Process

Boston Scientific's hybrid workplace includes remote and onsite roles. By applying to this position, you will have the opportunity to discuss your preferred working location with your Talent Acquisition Specialist.

Remote Eligible:  Onsite
Onsite Location(s): 

Maple Grove, MN, US, 55311

Hiring Manager: Chris Youssef Nazy
Recruiter: Spencer Gregory Hale

 

Process Engineer II

 

About the Role:

  • The candidate must be highly motivated and driven to solve technical/complex problems in both a hands-on manner and team setting, working in a fast-paced environment, and across multiple functions in a global company.  
  • Uses technical and collaboration skills alongside passion for innovation and continuous improvement to drive growth through efficient and effective commercialization of new products and targeted improvements.  
  • The successful candidate for this position will provide strong leadership and problem solving to enable medical device innovation. 
  • This position offers the opportunity to support process development and product commercialization throughout Boston’s global plant network.
  • Works cross-functionally to lead process development of complex technologies on new products, drive/develop new business activities and rapid prototyping execution and ensures efficient and effective transfer of product into production.

 

 

Your Responsibilities Will Include:

  • Applies technical knowledge to innovate, design, and develop processes, procedures, tooling and/or automation.
  • Assesses process capabilities, prioritizes process improvement opportunities, and innovates and implements process improvements on platform or derivative projects.
  • Executes the functional deliverables associated with the PDP/TDP, Project Management, and Quality Systems.
  • Partners with R&D to develop design specifications, test methods, and material selection
  • Provides Design for Manufacturability (DFM) input to the engineering print package.
  • Prepares and presents technical data and recommendations at technical reviews.
  • Ensures proper documentation is completed to meet quality systems requirements. (e.g., BOM’s, Routers, FMEA’s, etc.)
  • Writes and reviews validation protocols and reports applicable to new processes.
  • Oversees development builds associated with the project using special work requests.
  • Trains and/or provides work direction to technicians and engineers and may train manufacturing personnel when required as part of a validation.
  • Proposes or investigates new technologies
  • Contributes ideas to or generates Intellectual Property submissions.

 

What We’re Looking For In You:

Minimum Qualifications

  • BS in Engineering and 2-4 years of experience
  • Strong mechanical aptitude, conflict resolution and problem-solving skills.
  • Demonstrated ability to develop and drive innovative solutions into processes and products.
  • Demonstrated cross functional teamwork in technically demanding environment.
  • Strong communications and time management skills.
  • Open to travel up to 10% of time. 

 

Preferred Qualifications

  • Experience developing and characterizing various types of processes.
  • Experience with Catheter assembly.
  • Demonstrated use of DFSS tools (DOE, problem solving).
  • Demonstrated ability to develop equipment/fixtures/tooling from concept to production.
  • Experience with mechanical design.
  • Strong understanding of statistics and proficiency in Minitab.
  • Medical device or other regulated industry experience.

 

Requisition ID: 539572


Nearest Major Market: Minneapolis

Job Segment: Process Engineer, Medical Device Engineer, Business Process, Project Manager, Engineering, Quality, Technology, Management

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