Intern, CQV

Fujifilm

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profile Job Location:

Holly Springs, MS - USA

profile Monthly Salary: Not Disclosed
Posted on: 20 hours ago
Vacancies: 1 Vacancy

Job Summary

Position Overview

The Intern on the CQV team integrates into ongoing work supporting building out the needed processes for execution of testing reviewingdocumentation 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 well open North Americas largest end-to-end CDMO biopharmaceutical manufacturing facility offering drug substance production fill-finish and packaging under one roof.

Were 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 were proud to cultivate a culture that will fuel your purpose energy and drivewhat we call Genki. Ready to shape the future of medicine Lets transform healthcare together!


Holly Springs North Carolina combines small-town warmth with proximity to Raleighs thriving tech scene making it the perfect blend of community and opportunity.


Fujifilm is globally headquartered in Tokyo with over 70000 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: Description

What Youll Do

Under the direct supervision support and guidance of the manager:

Collaborates with manager and experienced Engineers on identified project(s). Creates and delivers presentation on identified project to SiteLeadership 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 DSMsystems 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 readinessactivities
Collaborate with CQV team to create methods to track the number of reviews taking place establishing a baseline for rework a target for reducingrework 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

Basic Requirements

Currently enrolled in an Associates Degree program with a LifeSciences focusOR
Currently enrolled in an Engineering or Scientific Undergraduate or Masters degree Program
Proficient in Microsoft Word Excel and PowerPoint
Wear the appropriate Personal Protective Equipment in an activeconstruction site

Preferred Requirements

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

WORKING CONDITIONS & PHYSICAL REQUIREMENTS

To all agencies: Please no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email the internet or in any form and/or method will be deemed the sole property of FUJIFILM unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired no fee or payment of any kind will be paid.

EEO Information

ADA Information


Required Experience:

Intern

Position OverviewThe Intern on the CQV team integrates into ongoing work supporting building out the needed processes for execution of testing reviewingdocumentation and partnering with our leads to identify and drive opportunities for improvement.Start Date:This internship is set to begin on May 26...
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