Validation Intern

Catalent Pharma Solutions • Greenville, NC

1d • Onsite

About The Position

Validation Intern Position Summary: Work Schedule: Maximum 28/h per week 100% based on-site in Greenville, NC 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

• Requires a High School Diploma or equivalent.
• Current or recent enrollment in an undergraduate or graduate degree program in Engineering or related technical discipline.
• Must be located within 50 miles of Greenville, North Carolina, site during internship to be considered.
• Some exposure to hazardous chemicals and other active chemical ingredients.
• Individual may be required to sit, stand, walk regularly, handle and manipulate objects using hands and arms.
• This position requires that a respirator be worn for your safety, and as such, employment is contingent upon being able to complete a medical evaluation with satisfactory results. The medical evaluation is conducted via an external vendor assigned by Catalent.

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.
• Other duties as assigned.

What This Job Offers

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