Intern, QA Operations DSM
About The Position
The QA Intern is responsible to assist in the Quality oversight of Drug Substance Manufacturing and supporting areas, bridging from site project/startup phase to operational readiness. The QA Intern collaborates within the Drug Substance Quality Operations team as well as with other project teams on site with a focus on consistent policy administration, QA oversight of day-to-day activities and resolution or mitigation of issues occurring during operation. 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. 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
- Supports QA for specific tasks and deliverables within the assigned Quality area
- Participates in streamlining and standardizing day to day quality related risks
- Maintain detailed schedules via Smartsheet, electronic and physical dashboards, and PowerPoint presentations as applicable
- Prepare and coordinate optimization of deliverables with other cross-functional stakeholders and internal customers.
- Accomplish assigned intern project tasks on agreed timelines
- Design/maintain a communication strategy to provide schedule, task, and status updates to the impacted teams.
- Other duties as assigned
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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
