Product Development Intern

Catalent • Greenville, NC

11h • Onsite

About The Position

Product Development Intern The Product Development Intern is an entry level, part-time position that will assist in project execution. Position Summary This position is 100% on-site at the Greenville site. 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 Role With close supervision support and assist in qualification of equipment. With close supervision, assist in dispensing operations. Become familiar with the QAD inventory system, and utilize system to dispense raw materials. With close supervision, assist in the development of timelines, Gantt charts and entry into MS Project. Research existing documents, and perform data entry and data analysis. Execute experiment documentation such as protocols and manufacturing records. With close supervision, assemble, disassemble, and clean and store equipment. Ensure that all work is accurate, precise, properly documented, and compliant with SOPs and FDA cGMP guidelines. All other duties as assigned.

Requirements

• Current or recent enrollment in an undergraduate or graduate degree program is required (e.g. Chemistry, Chemical Engineering, Mechanical Engineering, or Pharmaceutical Science).
• Proficient in Microsoft Word, Excel, and PowerPoint.
• Must be located within 50 miles of the Greenville, North Carolina, site during internship to be considered.
• 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

• Support and assist in qualification of equipment.
• Assist in dispensing operations.
• Become familiar with the QAD inventory system, and utilize system to dispense raw materials.
• Assist in the development of timelines, Gantt charts and entry into MS Project.
• Research existing documents, and perform data entry and data analysis.
• Execute experiment documentation such as protocols and manufacturing records.
• Assemble, disassemble, and clean and store equipment.
• Ensure that all work is accurate, precise, properly documented, and compliant with SOPs and FDA cGMP guidelines.
• All other duties as assigned.

What This Job Offers

• Job Type: Part-time
• Career Level: Intern
• Education Level: No Education Listed