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Senior QA Validation Engineer

Job Location:

Madison, OH - USA

Monthly Salary: Not provided by the employer

Posted: 22 August 2026 (10 hours ago)

Application Deadline: 19 November 2026

Vacancies: 1 Vacancy

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Job Summary

Position Overview

FUJIFILM Cellular Dynamics Inc. is seeking an expert in validation engineering who will apply knowledge of qualification and validation principles to manufacturing processes quality systems engineering design fundamentals regulatory authority expectations and industry standards as well as review and approve relevant documents. You will perform quality oversight of all validation for GMP including equipment facility and utility systems information technology computerized systems drug product manufacturing processes and methods.

Company Overview

At FUJIFILM Cellular Dynamics were unlocking the power of human cells to change lives. Using revolutionary induced pluripotent stem cell (iPSC) technology we drive advancements in drug discovery disease modeling cell therapy research tools and cell therapy manufacturing. Our mission is deeply meaningful and were looking for bold innovators to join us.

At FUJIFILM Cellular Dynamics youll thrive in a collaborative and cutting-edge environment that encourages creativity and celebrates breakthroughs. If youre ready to do work that makes a real impact and propels healthcare forward this is your chance to be part of something extraordinary for science patients and yourself.

Our headquarters is in Madison Wisconsin a dynamic city celebrated for its lakes parks cultural richness biotech leadership and access to world-class academia.

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

Essential Job Functions

Provide validation focused design and development by engaging with cross-functional teams to define requirements design verification and validation plan and strategies.
Serve as a best practices/quality resource on highly significant matters relating to policies programs capabilities and long-range goals and objectives.
Lead sub streams or participate in cross-functional project teams to solve complex problems by using analytical thinking tools and judgment to identify innovative solutions
Lead problem solving of complex issues where analysis of situations or data requires an in-depth evaluation of variable factors including cross-functional impact exercising sound judgment based on the analysis of multiple sources of information and interactions with peers and cross-functional teams.
Generate validation protocols (IQ/OQ/PQ) of all site equipment including laboratory equipment production equipment utilities (as applicable) and other related systems in a Health Authority regulated environment.
Generate validation strategy for OTS software and IT systems ensuring compliance with data integrity expectations.
Author and review SOPs protocols reports and validation master plans for GMP equipment instruments and computerized systems.
Perform risk assessments for GMP systems as required and plan validation efforts according to risk.
Train end users on validation policies and requirements to support GMP operations.
Collaborate with clients and vendors to meet project and company objectives.
Participate in audits and regulatory agency inspections for Validation.
Serve as subject matter expert in qualification and validation.
Troubleshoot and coordinate failure investigations for manufacturing and laboratory equipment.
Assist with vendor communications and maintenance/repair scheduling.
Resolve deviations and non-conformances reported during validation/qualification.
Assist with engineering studies and investigations in other departments and perform any additional responsibilities as requested or assigned.
Other duties as assigned.

Qualifications

Bachelors degree in a relevant field; advanced degree preferred.
A minimum of ten (10) years of relevant experience in technical and/or quality validation engineering with demonstrated progression in responsibilities.
Demonstrated organizational; problem solving; decision-making; communication (oral and written); and influencing skills dealing with diverse stakeholders.
Detailed focused with demonstrated writing and communication skills using MS Office.

Physical Requirements:

Able to work at a computer for extended periods of time.
Able to wear standard laboratory PPE.

EEO Information

Fujifilm is committedto providing equal opportunities in hiring promotion and advancement compensation benefits and training regardless of nationality age gender sexual orientation or gender identity race ethnicity religion political creed ideology national or social origin disability veteran status etc.

ADA Information

If you require reasonable accommodation in completing this application interviewing completing any pre-employment testing or otherwise participating in the employee selection process please direct your inquiries to our HR Department ().

Required Experience:

Senior IC

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About Company

Fujifilm

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