Intern - Quality Control
Listed on 2026-11-05
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
2027 Intern
- Quality Control
Position Summary:
- Shift: M-F 8am-5pm, Summer 2027
- Location:
Madison, WI - 100% Onsite
Catalent’s Madison, Wisconsin site is a state‑of‑the‑art biologics development and manufacturing facility supporting customers from research through early‑ and mid‑stage clinical production. Located at 726 Heartland Trail in Madison, the approximately 102,700‑square‑foot GMP facility specializes in mammalian cell line engineering, drug substance biomanufacturing, and biopharmaceutical development, utilizing flexible single‑use systems to enable rapid scale‑up and customization. The site is home to Catalent’s proprietary GPEx® and GPEx® Lightning technologies, which are used to generate high‑yielding mammalian cell lines for biologic therapies, and supports production scales ranging from 50 to 4,000 liters for clinical manufacturing.
Following a $45 million expansion announced in 2025, the Madison site has significantly increased capacity, added new equipment, and created approximately 200 highly skilled biohealth jobs, further strengthening its role within Catalent’s global biologics network and Wisconsin’s growing life sciences ecosystem.
- Quality Control to join our team and support Quality Control processes as assigned. You will assist with technical data collection, process improvements, and key project initiatives while learning and contributing to laboratory systems, databases, and documentation.
This role offers hands‑on experience in data organization, analysis, and reporting within a regulated environment. You will collaborate with team members, maintain compliance with safety and quality standards, and contribute to process improvement initiatives.
The Role
- Support Quality Control activities through data collection, documentation, and process improvement initiatives.
- Assist with laboratory systems, databases, reporting, and maintaining accurate records.
- Analyze, organize, and document data to support projects and operational objectives.
- Collaborate with cross‑functional teams, participate in meetings, and contribute to team projects.
- Ensure compliance with safety, quality, and 5S standards while completing assigned projects and presenting results.
The Candidate
Minimum Requirements
- Currently enrolled in an accredited college or university.
- Must be an undergraduate or graduate student pursuing a degree in life sciences such as Biology, Biochemistry, Molecular Biology, Microbiology, 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.
- Ability to read, understand, and apply standard operating procedures to operate within a regulated industry and compliance environment.
Why You Should Join Catalent
- Defined career path and annual performance review and feedback process.
- Diverse, inclusive culture.
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
- 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.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life‑saving and life‑enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting…
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