Boston Scientific
Manufacturing Engineer II
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 Manufacturing Engineer II will lead initiatives for the daily support of products, processes, materials, and equipment and drive production goals (i.e., safety, quality, delivery, cost, and productivity). This individual will be required to routinely partner with cross-functional teams to evaluate, troubleshoot and implement manufacturing processes within the business unit. Your responsibilities will include: Monitor performance of equipment, machines, and tools to correct equipment problems or identify issues within process that contribute to non-conforming parts, low yields, or product quality issues Perform troubleshooting on new and existing products/process problems as related to design, material, or processes Successfully contribute to business goals and product support, by utilizing tools such as process capability studies, process development, Six Sigma and Value Improvement projects, report preparation and process/test documentation Design and coordinate standard engineering tests and experiments Design, procure, and fabricate equipment tooling and fixtures Characterize the physical and material properties of the components, and optimize these properties against device performance requirements Summarize, analyze, and draw conclusions from test results Complete and manage Capital Expenditure Request and Authorizations (CERA's) Prepare standard reports/documents to communicate results to the technical community Lead cross-functional project teams as required Identify, implement, and manage equipment requirements to support production goals Work cooperatively with R&D, Process Development, Quality, Production, Regulatory, Equipment Engineering, Supply Chain, and Marketing to ensure project success Required qualifications: Bachelor's degree in engineering (preferably Manufacturing, Biomedical, Chemical, or Mechanical) 2+ years of relevant work experience in a manufacturing environment Proven understanding of manufacturing problem solving, data analysis, and production flow tools (i.e. LEAN manufacturing) Preferred qualifications: Experience in the medical device industry or other highly regulated industry Experience with polymer extrusion or other similar extrusion Project management experience Experience with validation and qualification of equipment Proven ability to drive process improvement initiatives Strong written and verbal communication skills with ability to develop and present ideas via visual communication methods
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 Manufacturing Engineer II will lead initiatives for the daily support of products, processes, materials, and equipment and drive production goals (i.e., safety, quality, delivery, cost, and productivity). This individual will be required to routinely partner with cross-functional teams to evaluate, troubleshoot and implement manufacturing processes within the business unit. Your responsibilities will include: Monitor performance of equipment, machines, and tools to correct equipment problems or identify issues within process that contribute to non-conforming parts, low yields, or product quality issues Perform troubleshooting on new and existing products/process problems as related to design, material, or processes Successfully contribute to business goals and product support, by utilizing tools such as process capability studies, process development, Six Sigma and Value Improvement projects, report preparation and process/test documentation Design and coordinate standard engineering tests and experiments Design, procure, and fabricate equipment tooling and fixtures Characterize the physical and material properties of the components, and optimize these properties against device performance requirements Summarize, analyze, and draw conclusions from test results Complete and manage Capital Expenditure Request and Authorizations (CERA's) Prepare standard reports/documents to communicate results to the technical community Lead cross-functional project teams as required Identify, implement, and manage equipment requirements to support production goals Work cooperatively with R&D, Process Development, Quality, Production, Regulatory, Equipment Engineering, Supply Chain, and Marketing to ensure project success Required qualifications: Bachelor's degree in engineering (preferably Manufacturing, Biomedical, Chemical, or Mechanical) 2+ years of relevant work experience in a manufacturing environment Proven understanding of manufacturing problem solving, data analysis, and production flow tools (i.e. LEAN manufacturing) Preferred qualifications: Experience in the medical device industry or other highly regulated industry Experience with polymer extrusion or other similar extrusion Project management experience Experience with validation and qualification of equipment Proven ability to drive process improvement initiatives Strong written and verbal communication skills with ability to develop and present ideas via visual communication methods