What are the responsibilities and job description for the Intern: DPFG MSAT Process Engineer position at FujiFilm and Careers?
The Drug Product and Finished Goods (DPFG) MSAT Intern will help setup the framework and systems of manufacturing process development and bioprocess data at FDBN.
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
Under the direct supervision, support and guidance of the manager:
Collaborates with experienced engineers on identified project(s). Creates and delivers presentation on identified project to Site Leadership Team at the conclusion of internship.- Builds up understanding of drug product and finished goods processes via daily process monitoring, in process control trending and data analysis
- Assists in the optimization of equipment and manufacturing processes
- Supports process issues and deviation investigations
- Supports the system and logistics for MSAT samples (for process comparability, stability studies and investigation)
- Ensures that all work is accurate, precise, properly documented, and compliant with SOPs and FDA cGMP guidelines
- Assists MSAT process engineers/experts in supporting drug product and finished goods manufacturing operations, as applicable
- Performs other duties, as assigned
Basic Requirements
Currently enrolled in an Associate's Degree program with a Life Sciences focus OR- Rising Junior or above and enrolled in an Engineering or Scientific Undergraduate or Master’s degree Program
- Proficient in Microsoft Word, Excel, and PowerPoint
Preferred Requirements
Prior experience in Pharma/Biotech/Chemical Industry is preferred- Prior hands-on technical experience (in a laboratory or manufacturing environment)
WORKING CONDITIONS & PHYSICAL REQUIREMENTS
- Ability to discern audible cues
- Ability to ascend or descend ladders, scaffolding, ramps, etc
- Ability to stand for prolonged periods of time - up to 60 minutes
- Ability to sit for prolonged periods of time - up to 240 minutes
- Ability to conduct activities using repetitive motions that include writs, hands and/or fingers
- Ability to conduct work that includes moving objects up to 10 pounds
EEO Information: