Intern (Disposables Engineering) - Allen
1 week ago

Job summary
Assist in sustaining manufacturing processes by supporting troubleshooting documentation and continuous improvement activities Assist execution of validation and qualification protocols for equipment processes and design changes Collaborate with engineers to identify and implement process improvements that enhance safety quality and throughput Participate in engineering change order ECO documentation test execution and implementation activities Help analyze production data perform basic statistical analysis summarize findings in reports Observe participate root cause analysis activities nonconformance investigations Learn apply Lean Six Sigma principles reduce waste improve efficiency Participate design reviews contribute DFM Design for Manufacturability input under guidance Assist drafting technical documents validation plans troubleshooting guides Learn quality regulatory standards applicable medical devices including FDA QSR ISO 13485 Education And Experience Requirements Pursuing Bachelor's degree Mechanical Industrial Manufacturing Biomedical Engineering related field Previous internship coop project experience regulated manufacturing medical device environment plus Required Skills And Abilities Strong organizational time management skills independently complete assigned tasks Strong interest medical device manufacturing continuous improvement Effective written verbal communication skills Detail oriented self motivated follow directions ask questions Familiarity Microsoft Office Excel PowerPoint exposure SolidWorks CAD preferred Basic understanding root cause analysis data analysis engineering documentation Seniority level Internship Employment type Full-time Job function Education Training Industries Machinery Manufacturing
Job description
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