Senior Process Engineer

Additional Location(s):  N/A

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.           

 

About the role:

 

Boston Scientific is looking for a highly motivated Senior Process Engineer 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. This position involves cross-functional collaboration to improve and commercialize new and existing TCAR (Transcarotid Artery Revascularization) 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.

  

Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.

  

Your responsibilities will include: 

 

• Assess process capabilities, prioritize process improvement opportunities, and innovate and implement process improvements on platform or derivative projects 

• Apply technical knowledge to innovate, design, and develop processes, procedures, tooling, and/or automation 

• Execute the functional deliverables associated with the PDP/TDP, Project Management, and Quality Systems 

• Write clean and concise work instructions that can be understood by product builders   

• Own 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 processes 

• Prepare and present technical data and recommendations at technical and business reviews using statistical best practices

• Provide Design for Manufacturability (DFM) input to the engineering print package 

• Partner cross-functionally to develop design specifications, test methods, and material selection     

• 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

  

Required qualifications:

 

• Bachelor’s degree in Engineering or related technical field 

• Minimum of 4 years of professional engineering experience relevant to this role, or minimum of 3 years of professional engineering experience relevant to this role with an advanced degree

• Hands-on mechanical aptitude  

• Demonstrated cross functional teamwork in a technically demanding environment 

• Strong written and verbal communication skills 
• Must be able to provide own, reliable transportation to commute effectively between Maple Grove sites (Weaver Lake and Arbor Lakes facilities)

 

Preferred qualifications:

 

• Bachelor’s degree in Biomedical, Mechanical, or Materials Science
• Prior experience in medical device industry or similar highly-regulated industry   

• Demonstrated use of standardized problem-solving or experimental tools  

• Experience developing and cha