Validation Intern

Catalent

8d • Onsite

About The Position

Validation Intern Position Summary · 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.

Requirements

• 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

Responsibilities

• 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

What This Job Offers

• Career Level: Intern
• Education Level: High school or GED
• Number of Employees: 5,001-10,000 employees