About the role#
This internship provides hands-on experience in a regulated pharmaceutical environment. You will support the Quality Control team by assisting with technical data collection, process improvements, and key project initiatives. You will work directly with laboratory systems and databases while learning to maintain accurate documentation and records.
What you'll do#
- Collect and organize data to support operational objectives and project goals.
- Assist with laboratory systems, reporting, and maintenance of accurate records.
- Collaborate with cross-functional teams and participate in regular meetings.
- Contribute to team projects and present your results.
- Ensure all work complies with safety, quality, and 5S standards.
What you'll need#
- Current enrollment in an accredited college or university.
- Pursuing an undergraduate or graduate degree in a life science field such as Biology, Biochemistry, Molecular Biology, or Microbiology.
- Ability to work full-time (40 hours per week) for a 12-week period during the summer.
- Capacity to read, understand, and apply standard operating procedures.
- Eligibility to legally work in the United States.
Location & details#
- Location: Madison, Wisconsin.
- Term: Summer 2027.
- Modality: 100% on-site.
- Employment: Full-time.
About Catalent
Catalent is a contract development and manufacturing organization based in Tampa, Florida. The company provides manufacturing and development services to pharmaceutical, biotechnology, and consumer health firms. It operates more than 40 sites globally and employs over 10,000 people. The company manages over 1,000 active development programs and produces more than 60 billion doses of medication each year.
How to get in at Catalent
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