2027 Intern - QA, QMS
Catalent Pharma Solutions
Summary
Shift: M-F 8am-5pm, Summer 2027. Location: Madison, WI. 100% Onsite.
Job description
Position Summary
Shift: M-F 8am-5pm, Summer 2027. Location: Madison, WI. 100% Onsite.
We have an opportunity for a 2027 Intern - QA, QMS to join our team and support Quality Systems projects and process improvement initiatives. The intern will assist with document control, data collection, and quality reporting while learning about electronic quality systems and compliance processes. This role offers hands-on experience in maintaining accurate records, supporting supplier quality activities, and contributing to continuous improvement efforts. The position provides exposure to cross-functional collaboration and real-world applications of quality management principles.
The Role
- 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, follow safety and compliance requirements, and present project updates and results.
The Candidate
- Currently enrolled in an accredited college or university.
- Undergraduate or graduate student pursuing a 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 a 12-week period 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.
Requirements
- Currently enrolled in an accredited college or university
- Undergraduate or graduate student pursuing a 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 a 12-week period 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
Benefits
- Paid Time Off
- 8 Paid Holidays
- Medical, Dental & Vision
- Tuition Reimbursement
- Career Growth
- Community Engagement
Company overview
Catalent Pharma Solutions, now known as Catalent, Inc., is a leading global contract development and manufacturing organization (CDMO) headquartered in Tampa, Florida. Founded in 2007 as a spin-off from Cardinal Health's pharmaceutical technologies segment, the company has grown into a major player in the pharmaceutical services industry. Catalent provides comprehensive drug development and manufacturing solutions including drug delivery technologies, formulation development, analytical testing, clinical and commercial manufacturing, clinical packaging, and supply chain services. The company operates over 50 facilities across four continents and has supported more than half of all FDA-approved products over the past decade. With approximately 16,900 employees, Catalent produces over 70 billion doses annually for more than 8,000 products, serving major pharmaceutical companies like Pfizer, Moderna, Novo Nordisk, and Bristol-Myers Squibb. In 2024, the company was acquired by Novo Holdings A/S for $16.5 billion, further strengthening its position in the global pharmaceutical manufacturing landscape.