Validation Intern

Validation Intern

100% on‑site

Catalent is a global, high‑growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Catalent’s Greenville, N.C. facility specializes in end‑to‑end turn‑key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state‑of‑the‑art facility has had over $100M of investments in recent years and features fit‑for‑scale capacity with potent handling capabilities, ideal for orphan or targeted drug development.

Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee.

Catalent’s Greenville, N.C. facility specializes in end‑to‑end turn‑key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state‑of‑the‑art facility has had over $100M of investments in recent years and features fit‑for‑scale capacity with potent handling capabilities, ideal for orphan or targeted drug development.

The Validation Intern provides direct validation support to pharmaceutical development, engineering, and manufacturing operations. With direction and supervision, performs activities related to validation and site projects as well as supporting quality functions to obtain both validation and pharmaceutical industry knowledge and skills to allow their growth and development for education or potential hire into a role in the pharmaceutical industry.

• Learn about cGMPs and the Pharmaceutical Business
• Learn Basic Principles of Validation:
  Process, Equipment, Cleaning, Facilities, Utilities, and Packaging
• Sample and test for cleaning, process, and packaging
• Assist with Validation protocol execution – all types
• Analysis of Data
• Reviews Protocols and Reports for Calculations, Spelling, Grammar, and presence of support documentation.
• May be assigned to assist with special department or site projects. This list is not all inclusive

• High school diploma or equivalent required
• Current or recent enrollment in an undergraduate or graduate degree program (e.g. Life Sciences, Physics or Engineering)
• Must be located within 50 miles of the Greenville, North Carolina, site during internship to be considered
• Some exposure to hazardous chemicals and other active chemical ingredients
• Position requires the capacity to handle and manipulate objects using hands and arms

• Spearhead exciting and innovative projects
• Fast‑paced, dynamic environment
• High visibility to members at all levels of the organization

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.

Visit Catalent Careers to explore career opportunities.

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 Disabili 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 to the application or hiring process.

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