About The Position
This internship focuses on Document Control within the Quality department, providing hands-on experience in organizing and managing GMP documents. The intern will work with cross-functional departments, utilizing tools like Word, Excel, and PowerPoint. This role is crucial for understanding the importance of documentation in the pharmaceutical industry.
Requirements
- High School diploma or GED.
- Current full-time enrollment in an accredited college or university undergraduate or graduate program in Human Resources, Business Administration, Psychology, or a related field.
- Minimum cumulative GPA of 3.0.
- Must be at least 18 years old.
- Must be legally authorized to work in the United States.
- Must commit to the full duration of the internship (June 1, 2026 - August 28, 2026).
Nice To Haves
- Strong typing skills.
Responsibilities
- Organizing and prioritizing GMP documents.
- Working with printers and scanners.
- Utilizing Word, Excel, and PowerPoint.
- Collaborating with cross-functional departments.
Benefits
- Paid internships
- Rates starting at $20/hr
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What This Job Offers
Career Level
Intern
Education Level
High school or GED
Number of Employees
1,001-5,000 employees
