2027 Intern - QA, QMS

Catalent Pharma Solutions • Madison, WI

2d • Onsite

About The Position

Catalent’s Madison, Wisconsin site is a biologics development and manufacturing facility supporting research through early- and mid-stage clinical production. The site specializes in mammalian cell line engineering, drug substance biomanufacturing, and biopharmaceutical development, with production scales from 50 to 4,000 liters for clinical manufacturing.

The 2027 QA, QMS Intern will support Quality Systems projects and process improvement initiatives. The role involves document control, data collection, quality reporting, and exposure to electronic quality systems and compliance processes. The intern will help maintain accurate records, support supplier quality activities, and contribute to continuous improvement while collaborating across functions and applying quality management principles.

This is a 12-week summer 2027 internship, working 40 hours per week, Monday through Friday, 8:00 a.m. to 5:00 p.m. It is 100% onsite in Madison, Wisconsin.

Requirements

• Currently enrolled in an accredited college or university.
• Pursuing an undergraduate or graduate degree in Quality Assurance, Biology, Chemistry, Biochemistry, Engineering, Pharmaceutical Sciences, Life Sciences, Business Administration, Information Systems, or a related field.
• Ability to work full-time (40 hours per week) for 12 weeks over the summer.
• Basic proficiency with Microsoft Office applications, including Excel, Word, PowerPoint, and Outlook.
• Strong attention to detail and ability to manage documentation accurately.
• Ability to analyze information, follow procedures, and maintain confidentiality of quality records.

Responsibilities

• Support Quality Systems projects, process improvements, and automation initiatives.
• Assist with document control, record management, and maintenance of quality system documentation.
• Collect, analyze, and report quality data, metrics, training compliance, and supplier performance information.
• Maintain accurate records and support equipment, training, and supplier quality management activities.
• Collaborate with cross-functional teams and follow safety and compliance requirements.
• Present project updates and results.

Benefits

• Defined career path and annual performance review and feedback process.
• Diverse, inclusive culture.
• Potential for career growth on an expanding team.
• Competitive paid time off plus 8 paid holidays.
• Community engagement and green initiatives.
• Medical, dental, and vision benefits effective day one of employment.
• Tuition reimbursement.

What This Job Offers

• Job Type: Full-time
• Career Level: Intern
• Education Level: No Education Listed