Intern, QC Chemistry
About The Position
The QC Chemistry Intern will lead and execute a targeted project focused on Total Organic Carbon (TOC) analysis to support a defined stability study protocol. The role performs routine and study-specific TOC testing of cleaning verification samples and standards to extend expiry dates of pre-prepared TOC kit materials. The analyst develops and maintains study documentation and collaborates with Quality Control Leadership on conclusions drawn from the study results. This role exists to increase overall laboratory workload efficiency for the preparation, processing, and testing of cleaning verification samples. Start Date: This internship is set to begin on May 26th 2026 for an 11-week duration ending on August 7th 2026. Relocation: Please note this Internship Opportunity is designed to be 100% Onsite, 40 hours/week and a relocation/housing stipend is not provided. Company Overview FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we’ll open North America’s largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof. We’re looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we’re proud to cultivate a culture that will fuel your purpose, energy, and drive—what we call Genki. Ready to shape the future of medicine? Let’s transform healthcare together! Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh’s thriving tech scene, making it the perfect blend of community and opportunity. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: https://www.fujifilm.com/us/en/about/region/careers
Requirements
- Currently enrolled in an Associate's Degree program with a Life Sciences focus OR
- Currently enrolled in an Engineering or Scientific Undergraduate or Master’s degree Program
- Proficient in Microsoft Word, Excel, and PowerPoint
Nice To Haves
- Prior experience in Pharma/Biotech/Chemical Industry
- Prior hands-on technical experience (in a laboratory or manufacturing environment)
Responsibilities
- Performs and documents TOC analyses using validated instruments under current Good Manufacturing Practices (cGMP) in the Quality Control Chemistry Laboratory
- Plans and executes TOC stability study per approved protocols and SOPs
- Trains on and reviews SOPs, sampling plans, protocols, and final study reports
- Authors training materials based on study results
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What This Job Offers
Job Type
Full-time
Career Level
Intern
Education Level
Associate degree
Number of Employees
501-1,000 employees
