2027 Intern - Quality Control

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

Benefits offered by this job

Defined career path and performance/反馈

Diverse, inclusive culture

Career growth on expanding team

Paid time off + 8 paid holidays

Tuition Reimbursement

Medical, dental, vision benefits from

Job summary

Catalent's Madison, Wisconsin site is seeking an energetic 2027 Intern for Quality Control to support data collection, documentation, and process-improvement initiatives. You will learn laboratory systems, databases, and documentation within a regulated environment and collaborate with cross-functional teams.

The role emphasizes safety, quality, and 5S standards while contributing to projects and presenting results.

Qualifications

• Currently enrolled in an accredited college or university.
• Undergraduate or graduate student pursuing a degree in life sciences such as Biology, Biochemistry, Molecular Biology, Microbiology, or related field.
• 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 in a regulated environment.

Responsibilities

• 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.

Skills

SOP proficiency

Data collection

Team collaboration

Education

Pursuing life sciences degree

Job description

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.

We have an opportunity for a 2027 Intern - 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 on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [e-mail]. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting.

Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to [e-mail] for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.

Volunteer Work Disclosure:

Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.

Massachusetts Lie Detector Test Notice:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.