Engineering Intern

At Jabil (NYSE: JBL), we are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, supply chain, and manufacturing solutions. With 60 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe.

Job Summary
The Intern provides support for day-to-day activities within the assigned function while gaining practical experience in a professional workplace environment. The role focuses on learning standard operational processes, safety practices, and quality requirements while contributing to team and organizational efficiency.

The Engineering Intern at Jabil's Monument site will support engineering activities within a highly regulated medical-device manufacturing environment. This role provides hands-on experience working in a cleanroom production setting, supporting engineers in process improvement, documentation, validation, and day-to-day manufacturing support. Interns will collaborate closely with cross-functional teams including Operations, Quality, R&D, Facilities, and EH&S.

• 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.

• 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.

• 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.