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2027 Intern - EHS&S

Catalent Pharma Solutions

Madison, WIOnsitePosted 19 days ago
InternshipInternOperations & Supply ChainCDMO
Original posting ↗

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. We have an opportunity for a 2027 Intern - EHS&S to join our team and support environmental, health, safety, and sustainability initiatives across the Madison site. The intern will assist with inspections, audits, and data analysis to help maintain compliance and drive continuous improvement. This role offers hands-on experience in environmental compliance, risk assessment, and safety culture development.

Job description

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. We have an opportunity for a 2027 Intern - EHS&S to join our team and support environmental, health, safety, and sustainability initiatives across the Madison site. The intern will assist with inspections, audits, and data analysis to help maintain compliance and drive continuous improvement. This role offers hands-on experience in environmental compliance, risk assessment, and safety culture development.

The Role

  • Support EHS&S programs through inspections, audits, field observations, and environmental compliance activities across site operations.
  • Collect, analyze, and report safety, environmental, sustainability, and corrective action metrics to support continuous improvement.
  • Assist with risk assessments, hazard analyses, incident investigations, and implementation of corrective and preventive actions.
  • Develop and maintain EHS&S documentation, training materials, communications, and audit-ready records in compliance with Good Manufacturing Practice and regulatory requirements.
  • Collaborate on cross-functional projects, emergency preparedness activities, and internship initiatives while maintaining 5S and workplace safety standards.

The Candidate

Minimum Requirements

  • Currently enrolled in an accredited college or university.
  • Undergraduate or graduate student pursuing a degree in Environmental Health and Safety, Occupational Safety, Environmental Science, Industrial Hygiene, Engineering, Biology, Chemistry, Biotechnology, Public Health, Security, Emergency Management, 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.
  • Completion of foundational coursework relevant to environmental, health, safety, security, sustainability, science, engineering, or regulated operations is preferred.
  • Basic knowledge of Microsoft Word, Excel, PowerPoint, and Outlook, with the ability to learn site systems and reporting tools.
  • Ability to read and follow written procedures, safety requirements, technical documents, and supervisor instructions.
  • Ability to appropriately handle confidential, compliance-related, and business-sensitive information.

Requirements

  • Currently enrolled in an accredited college or university.
  • Undergraduate or graduate student pursuing a degree in Environmental Health and Safety, Occupational Safety, Environmental Science, Industrial Hygiene, Engineering, Biology, Chemistry, Biotechnology, Public Health, Security, Emergency Management, 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.
  • Completion of foundational coursework relevant to environmental, health, safety, security, sustainability, science, engineering, or regulated operations is preferred.
  • Basic knowledge of Microsoft Word, Excel, PowerPoint, and Outlook, with the ability to learn site systems and reporting tools.
  • Ability to read and follow written procedures, safety requirements, technical documents, and supervisor instructions.
  • Ability to appropriately handle confidential, compliance-related, and business-sensitive information.

Benefits

  • Paid time off
  • 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.

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