Automation Engineering Intern — Summer 2027 (Onsite)

Catalent Pharma Solutions LLC; Madison (WI); On-site; USD 25,000 - 39,000; Full time

Job summary

Catalent Pharma Solutions LLC in Madison, WI is seeking a 2027 Intern - Engineering, Automation to support automation projects and assist with operational technology troubleshooting and system maintenance during the summer. This hands-on role provides exposure to system design, data collection, and documentation in a GMP environment.

You will work full-time for 12 weeks, 40 hours per week, onsite, with cross-functional collaboration and a focus on safety, quality, and 5S.

Qualifications

• Currently enrolled in an accredited college or university.
• Undergraduate or graduate student pursuing a degree in Engineering or a related field of study.
• Eligible to legally work in the United States.
• Ability to work full-time (40 hours per week) for a 12-week period over the summer.
• Familiarity with industrial or laboratory control systems.
• Ability to read electrical and instrumentation drawings.

Responsibilities

• Support automation and operational technology projects, including troubleshooting, maintenance, and system design activities.
• Collect, analyze, document, and maintain accurate data and records in compliance with company procedures.
• Follow all safety, quality, compliance, and departmental standards while maintaining 5S workplace organization.
• Collaborate with team members and cross-functional partners, actively participating in meetings and project discussions.
• Contribute to process improvement and automation initiatives while completing assigned projects and presenting progress or results.

Skills

Control systems familiarity

Electrical drawings reading

Education

Engineering or related field

Job description

Catalent Pharma Solutions LLC in Madison, WI is seeking a 2027 Intern - Engineering, Automation to support automation projects and assist with operational technology troubleshooting and system maintenance during the summer. This hands-on role provides exposure to system design, data collection, and documentation in a GMP environment.

You will work full-time for 12 weeks, 40 hours per week, onsite, with cross-functional collaboration and a focus on safety, quality, and 5S.