Validation Intern

Catalent Pharma Solutions•Greenville, NC

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.

Benefits

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