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The job in short
Engineering co-op supporting medical device supply management and manufacturing improvement.
Excel
Details
- Found
- 10 d ago · posted 2026-10-14
- Location as listed
- Indianola, PA,US, US
- Role
- Intern / Trainee
- Source
- The company’s own careers site
Full description
Support the External Supply Management Medical Device team on projects including product transfers, continuous improvement initiatives, and design upgrades; Conduct and document technical activities while working independently when required; Troubleshoot and resolve technical issues, determine next steps, and communicate recommendations to responsible engineers; Conduct project management activities, testing and trial work, analyze results, communicate observations and conclusions both verbally and in writing, and provide recommendations for next steps; Improve production processes and manufacturing techniques to meet cost of goods sold (COGS) and quality targets; Apply engineering principles and technical knowledge to support projects, drive results, and effectively communicate progress with project teams; Support engineers with operations management activities and manufacturing initiatives. Required: Demonstrated hands-on mechanical skills through coursework and/or extracurricular activities; Currently pursuing a bachelor's or graduate degree in Plastics Engineering, Mechanical Engineering, Biomedical Engineering, Bioengineering, Chemical Engineering, or a related engineering discipline; Must be entering sophomore through graduate year of college; Ability to generate and/or execute test methods and protocols; Strong customer focus with both internal and external stakeholders; Strong written, verbal, and presentation skills; Ability to independently develop ideas and solutions; Strong attention to detail, goal-oriented mindset, and demonstrated work ethic; Proficiency with Microsoft Office applications, including Teams, Word, Excel, Visio, and PowerPoint; Ability to work effectively within a team environment. Previous internship, co-op, laboratory, manufacturing, or engineering project experience; Experience working in a regulated manufacturing environment; Familiarity with medical device manufacturing processes and continuous improvement methodologies.