Intern, CQV

Fujifilm•Holly Springs, NC

1d•Onsite

About The Position

Position Overview The Intern on the CQV team integrates into ongoing work, supporting building out the needed processes for execution of testing, reviewing documentation, and partnering with our leads to identify and drive opportunities for improvement. 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 Job Description What You’ll Do Under the direct supervision, support and guidance of the manager:

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
Wear the appropriate Personal Protective Equipment in an active construction site

Nice To Haves

Prior experience in Pharma/Biotech/Chemical Industry
Prior hands-on technical experience (in a laboratory or manufacturing environment)

Responsibilities

Collaborates with manager and experienced Engineers on identified project(s).
Creates and delivers presentation on identified project to Site Leadership Team at the conclusion of internship.
Works with guidance and direction of CQV leadership to assess and develop the rationale for equipment family validation approach across DSM systems and revise the validation project plans (VPP)
Assists with improvements to the methods by which CQV plans and tracks execution of activities over time
Assists with tracking progress of post-approval of CQV protocols
Participates in mechanical completion walk downs in the construction field, assist the STW teams in field walkdowns and shakedown readiness activities
Collaborate with CQV team to create methods to track the number of reviews taking place, establishing a baseline for rework, a target for reducing rework, and suggestions on how to achieve the target
Assists the VTOP/CTOP readiness teams with progress tracking the document packages from the CM team
Identifies needs for Continuous improvement, by gathering feedback from users and implement improvement ideas for assigned projects
Performs other duties, as assigned