Position Overview Help build and optimize a best-in-class LabWare LIMS v8 environment that powers Quality Control in a GMP setting. As Sr. Specialist 1, QC LIMS, you'll configure, validate, and sustain a critical system that enables compliant, efficient testing—directly impacting product quality and patient safety. 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."

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https://www.fujifilm.com/us/en/about/region/careers Job Description About Us We are a collaborative Quality Control LIMS team partnering closely with Quality Control, Analytical Development, Manufacturing, IT, and Quality Assurance. Our mission is to ensure our LabWare LIMS operates in a robust, validated, and compliant state aligned with c

GMP, ICH, FDA, 21 CFR

Part 11, and GAMP expectations. We value curiosity, accountability, and cross-functional partnership, and we foster an inclusive environment where every voice is heard and respected. Minimum qualifications (must-have) Bachelor's degree in Computer Science, Information Technology, Biology, Microbiology, Biochemistry, or a related scientific discipline with 2+ years of experience; or Master's degree in the same fields with 0 years of experience Ability to function in a fast-paced, highly technical environment Demonstrated ability to work cross-functionally and build strong partnerships across levels (management, laboratory personnel, plant personnel) Thorough knowledge of c

GMP/ICH/FDA

regulations; familiarity with 21 CFR Part 11 and GAMP Strong verbal and written communication, technical writing, and problem-solving skills Understanding of pharmaceutical/biotech testing cycles or requirements Ability to work effectively with diverse teams Preferred qualifications (nice-to-have) 1-3 years of experience in a cGMP Quality Control department or FDA-regulated industry (drugs/biologics) Previous experience with LabWare LIMS development or other LIMS software development Experience with 21 CFR Part 11 and GAMP (applied/working experience) TrackWise (or similar quality system) experience for at least 1 year Leadership aptitude Responsibilities Participate in the LabWare LIMS v8 site go-live, including static data migration, configuration, validation, and cross-functional coordination to ensure a successful rollout. Collaborate with business subject matter experts to define and document new or revised LabWare requirements. Configure basic and advanced LabWare LIMS objects, including: Specifications, Analyses, Batch Templates, Test Lists, QC Samples Calculations, Format Calculations Templates (Stability, Sample Login, Standards, Reagents) Execute qualification/verification testing to support implementation of new or revised LabWare configurations. Maintain and, when needed, repair configuration objects within LabWare LIMS. Create queries to support evolving business requirements. Use the change management system to update configurations for specifications, analyses, and other static data in LIMS. Provide timely user support and troubleshooting; create new configuration templates; maintain accurate change records per version control procedures. Deliver LIMS training, technical support, problem reporting, and resolution for QC, QA, AD, and Manufacturing teams. Evaluate LIMS data to provide ad hoc and long-term reporting solutions; identify process gaps and propose improvements. Write test scripts for new LIMS functionality and participate in validation of new functionality/releases. Develop and maintain process configurations based on end user procedures and requirements. Partner with the LIMS team, IT, and end users to ensure new functionality meets user requirements.

Create and revise LIMS documentation:

SOPs, Work Instructions, Design Specifications, and training materials. Support LIMS platform expansion by preparing and executing validation test scripts. Liaise with laboratory end users to ensure configuration changes meet user needs. Revise or develop Functional Requirement Specifications (FRS) and User Requirement Specifications (URS), plus other relevant documentation. Perform other related duties as assigned. Work environment and physical requirements Ability to sit for prolonged periods (approximately 240 minutes daily); perform repetitive motions with wrists/hands/fingers. Ability to lift/move objects up to 10 lbs. Ability to discern audible cues and perform tasks requiring 20/20 corrected vision, including color differentiation. No routine requirement for respiratory protection, working at heights, operating motor vehicles/PITs, or working in extreme temperatures. Benefits We offer a competitive, comprehensive benefits package designed to support your well-being and growth.

Highlights typically include:

Competitive compensation with performance recognition Medical, dental, and vision coverage Retirement savings plan with company contribution Paid time off, company holidays, and paid parental leave Education assistance, professional development, and training Employee assistance program and wellness resources Inclusive culture with employee resource groups and opportunities to contribute to continuous improvement Equal Opportunity We are an equal opportunity employer. We welcome applicants of all backgrounds and are committed to a fair, accessible, and inclusive hiring process. If you require a reasonable accommodation at any stage, please let us know.

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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).