Engineering Intern at Jabil in Monument, CO

Summary: Jabil is a trusted partner for the world's top brands, offering comprehensive engineering and manufacturing solutions. The Engineering Intern will support engineering activities in a regulated medical-device manufacturing environment, gaining hands-on experience while assisting with process improvement and documentation. Responsibilities: - Assist Manufacturing and Process Engineers with daily floor support, including troubleshooting equipment, documenting issues, and participating in root cause analysis - Support time studies, workflow analysis, and process observations to identify improvement opportunities - Collect and analyze data to support engineering decisions, lean activities, and process optimization - Update or draft work instructions, standard operating procedures (SOPs), and engineering documentation under guidance - Participate in engineering change orders (ECOs), material dispositioning, and deviation management - Support completion of device history records (DHR) and ensure compliance with FDA and ISO 13485 requirements - Support continuous improvement initiatives aligned with Lean, Six Sigma, and Jabil Operating System (JOS) methodologies - Assist with equipment qualification and validation activities (IQ/OQ/PQ), including data collection and report drafting - Support small-scale engineering projects to reduce scrap, improve cycle time, or enhance product quality - Work closely with cross-functional partners such as Quality Engineering, Operations, Facilities, Tooling, and Supply Chain - Present project updates to engineering leaders and contribute findings during team meetings Required Qualifications: - Currently a Junior or Senior pursuing a bachelor's degree in mechanical engineering, Manufacturing Engineering, Biomedical Engineering, Industrial Engineering, or related field - Strong analytical, organizational, and documentation skills - Ability to work effectively in a regulated, fast-paced manufacturing environment - Proficient in Microsoft Excel, Word, and PowerPoint Preferred Qualifications: - Previous internship or hands-on engineering experience in manufacturing or medical devices - Familiarity with FDA regulations, ISO 13485, or GMP environments - Experience with CAD (SolidWorks, Creo, or similar) - Exposure to Lean Manufacturing or Six Sigma methodologies Required Skills: Manufacturing engineering, Medical device manufacturing, Process improvement, Validation, Manufacturing support, Microsoft Excel, Microsoft Word, Microsoft PowerPoint, FDA regulations, ISO 13485, GMP environments, CAD, Lean Manufacturing, Six Sigma, Analytical skills Benefits: Medical, dental, and vision insurance plans, 401(k) retirement plan, Employee stock purchase plan, Paid time off