QA Specialist, PQS

Fujifilm • Holly Springs, NC • 1d ago

Position Overview

The QA Specialist, PQS is responsible for the day-to-day activities of the Pharmaceutical Quality Systems team. This role requires system expertise and business knowledge to act as point of contact and maintain deep understanding of the system and process functionality/improvements and how they apply locally and globally to the system(s). The role collaborates and establishes relationships with site-based customers and global colleagues and provides updates to leadership as requested. As a system SME, the QA Specialist, PQS assists with user management, user support, problem solving and system training.

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

Supports QA for project deliverables in accordance with the governing processes, and procedures within the assigned Quality area

Assesses the impact of system controls and process modifications and maintains oversight of change management processes

Provides Quality/GMP oversight and approval of assigned area/systems and processes lifecycle documentation, including risk and impact assessments, product, process and equipment specifications, functional specifications, traceability matrices, qualification protocols, validation plans, and validation summary reports

Reviews and approves QA procedures for the validation approach and lifecycle documents as assigned

Generates, reviews, and approves QA documentation, procedures, and processes for operational readiness objectives and QA support of assigned area/systems in cGMP regulated facility

Ensures project and operational quality objectives are met within desired timelines

Actively seeks opportunities to collaborate and align with other FUJIFILM Diosynth Biotechnologies sites to streamline processes and maximize efficiency

Supports quality decisions that may impact operations, ensuring appropriate escalation

Identifies risks and communicates gaps for quality and GMP process/systemsPerforms other duties, as assigned

Minimum Requirements:

BS/BA in Life Sciences or Engineering or equivalent with 2+ years of applicable industry experience OR

Masters in Life Sciences or Engineering with 0 years of applicable industry experience.

1-3 years of experience in a GMP environment

Preferred Requirements:

Prior experience working within a QA role preferred

Working Conditions & Physical Requirements:

Will work in environment which may necessitate respiratory protection X No Yes

May work in Mechanical/Production spaces that may require hearing protection and enrollment in a hearing conservation program. X No Yes

Will work in environment operating a motor vehicle or Powered Industrial Truck. X No Yes

Ability to discern audible cues. No x Yes

Ability to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color. X No Yes

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 place. 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

Fujifilm is committed to 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 (FDBN_PNC@fujifilm.com).

Job Locations US-NC-Holly Springs

Posted Date 6 minutes ago (1/11/2026 9:31 PM)

Requisition ID 2026-36673

Category Quality Assurance

Company (Portal Searching) FUJIFILM Biotechnologies

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