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The Senior Project Manager, Strategy & Execution leads high-impact, cross-functional projects and strategic initiatives that advance the site’s operational and business strategy. This role sets the standard for project management excellence and cross-functional collaboration, translating strategy into executable roadmaps, establishing governance and delivery discipline, and ensuring benefits realization. The position partners closely with Site Leadership and functional leaders (Operations, Quality, EHS, Supply Chain, Finance, IT, HR) to prioritize, plan, and deliver initiatives on time, within scope and budget, while building project management capability and a culture of accountability across the site.
The Senior Project Manager, Strategy & Execution leads high-impact, cross-functional projects and strategic initiatives that advance the site’s operational and business strategy. This role sets the standard for project management excellence and cross-functional collaboration, translating strategy into executable roadmaps, establishing governance and delivery discipline, and ensuring benefits realization. The position partners closely with Site Leadership and functional leaders (Operations, Quality, EHS, Supply Chain, Finance, IT, HR) to prioritize, plan, and deliver initiatives on time, within scope and budget, while building project management capability and a culture of accountability across the site.
Make a meaningful impact at the intersection of biomanufacturing and digital operations. If you’re excited to learn and grow while supporting cGMP production with modern tools like MES, data historians, and electronic logbooks, this role is a great entry point into a high-impact, highly collaborative environment.
Summary: The Project Engineer, under the supervision of the Director of Engineering, will be responsible for leading, preparing, coordinating and monitoring the implementation of the assigned engineering projects including the development of any specifications and infrastructure requirements, discussion with A&E firms, project documentation review, contractors and/or vendor coordination, field progress inspection and project closeout documentation on behalf of the different facilities at Fujifilm Diosynth Biotechnology Texas (FDBT). Assigned projects may be related to new product introductions, local capital projects and/or strategic projects as dictated by business needs. This position will work closely with facilities, manufacturing resources, CAPEX team, validation, QA/QC, contractors and other functional areas to execute and document the projects Change Controls procedures as the main system for documenting changes to the facility, utility and/or equipment as applicable. This position will also support P&IDs development, maintenance strategies development, SOP’s development and equipment commissioning/qualification activities as required.
Summary: The Sr Compliance Specialist - Facilities Engineering, ensures that facilities, utilities, and critical systems operate in full compliance with applicable regulations, codes, and internal quality standards. This role leads and manages deviations, corrective/preventive actions (CAPA’s), effectiveness check, and change controls; maintains robust documentation and training programs. The Sr Compliance Specialist partners with Engineering, EHS, Quality, and Operations to sustain a state of control, optimize compliance processes, and ensure timely closure of records.
The Analyst, Quality Control (QC) All QC Team is responsible for performing routine testing requited for Urgent/STAT testing of manufacturing batch samples, clean utility, environmental monitoring. This role is part of a 24x7 team that supports testing/sampling across all of the QC laboratories required for urgent testing/Manufacturing support. The role will learn and perform testing/sampling across multiple labs in QC.
The Sr. Analyst 1, Quality Control (QC) All QC Team is responsible for performing routine testing required for Urgent/STAT testing of manufacturing batch samples, clean utility, environmental monitoring. This role is part of a 24x7 team that supports testing/sampling across all of the QC laboratories required for urgent testing/Manufacturing support. The role will learn and perform testing/sampling across multiple labs in QC.
FUJIFILM Electronic Materials, U.S.A., Inc., is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our Mesa, Arizona facility for a Document Control and Training Administrator!
The Role
The Document Control and Training Administrator supports manufacturing, warehouse, labs, maintenance & engineering, EHS, quality and other administrative department requirements for training and document control systems. They assist in managing documents, training, and support of day to day activities supporting the organization.
Build life-changing medicines with a team that trusts you to lead on the manufacturing floor. As a Manufacturing Associate 3 (Drug Substance Manufacturing), you’ll take ownership of critical processing steps, help bring new capacity online, and keep a 24/7 operation running safely, compliantly, and on time. If you thrive in hands-on, fast-paced environments and enjoy guiding others, this is your next step.
FUJIFILM Electronic Materials, U.S.A., Inc., is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our Mesa, AZ facility for a Software Automation Engineer!
The Role
This role will require a Software Automation Engineer with a customer-focused mindset, excellent organizational skills, and the flexibility to communicate across different time zones and business units, including occasional off-hour coordination and streamlining processes. The successful candidate will play a critical role in continuous improvement and maintaining high standards of data integrity while automating the current environment. A proactive mindset to manage and maintain the Certificate of Analysis (COA) and Electronic Certificate of Analysis (eCOA) systems within a complex, multi-system environment is necessary.
This role is responsible for coordinating and executing change requests, managing customer notifications including first batch reporting and the Advanced Shipping Notifications (ASN) communications, alongside ensuring accurate and timely data flow between ERP, LIMS, SAP, and third-party systems.
FUJIFILM Electronic Materials, U.S.A., Inc., is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our Pueblo, CO facility for a Warehouse Technician!
The Role
The Warehouse Technician will ship and receive hazardous chemicals according to all quality and ISO 45001, 9001 standards, and by following all DOT and CFR49 requirements. This is a 2nd shift opportunity. Must be able to work Monday through Friday, 10:00 AM - 6:30 PM.
FUJIFILM Cellular Dynamics is a leader in human iPSC-derived products and services that support disease modeling, drug discovery, and toxicology/safety pharmacology. The Director of Product Marketing will lead portfolio strategy and commercialization for the product offering, including cardiovascular, neural, endothelial, hepatic, immune, and other emerging cell models, associated media, assay and related offerings. This role is responsible for defining portfolio strategy, market positioning and communication strategy, lifecycle management, pricing, launch excellence, and go-to-market execution to accelerate growth, strengthen market leadership, and ensure the portfolio meets evolving customer and application needs across pharma, biotech, and academic research markets.
Help deliver safe, high-quality medicines at scale. As a Manufacturing Associate 3, Drug Product, you’ll play a hands-on role in component/parts preparation, thawing and formulation, sterile filling, and visual inspection—supporting a 24/7 operation that keeps patients at the center.
FUJIFILM Electronic Materials, U.S.A., Inc., is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our Mesa, AZ facility for a UI5 Solutions Architect Lead!
The Role
This role is responsible for supporting and managing the Electronic Batch Sheet System (SAP MII) and key users within FEUS. The Lead will drive the implementation of new development and improvement projects aimed at automating manual data entry and data manipulation processes to meet evolving customer demands. The position requires occasional travel across all sites.
As a leadership role, it involves guiding and mentoring team members to achieve excellence, providing weekly updates to the Applications Manager, and demonstrating exceptional interpersonal and organizational skills to manage distributed teams and effectively liaise with stakeholders at all levels.
FUJIFILM Electronic Materials, U.S.A., Inc., is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our Mesa, AZ facility for a Solutions Architect II!
With state-of-the-art manufacturing facilities in the U.S., Europe, Taiwan, China, Korea and Japan, local sales offices throughout the world and on-site applications support, FUJIFILM Electronic Materials supplies the world's top tier semiconductor manufacturers with a broad array of products and services used throughout the semiconductor manufacturing process.
The Role
We are seeking an experienced SAP MII/UI5 Solutions Architect to design, develop, and optimize complex full-stack web applications. The ideal candidate will bring strong technical expertise in both front-end and back-end development, delivering scalable and maintainable solutions.
This role requires close collaboration with cross-functional teams to build enterprise-grade applications and actively contribute to process improvements and best practices throughout the development lifecycle.
FCDI is seeking a Senior Analytical Development Scientist to support the company’s continued growth and several ongoing projects within the Analytical Development (AD) team located in Madison, Wisconsin.
The AD team works cross-functionally to design, develop, optimize, qualify, and validate analytical methods used to characterize and release a diverse portfolio of induced pluripotent stem cell (iPSC)-derived cell therapy products for ocular, oncological, neurological, and other diseases.
We are seeking an experienced, self-motivated, and detail-oriented scientist who can serve as a technical authority within the analytical development team for method transfer and development in preparation for qualification and validation. In this hands-on laboratory role, you will collaborate closely with Analytical Development leadership, method validation and senior technical staff to ensure that methods are adequately prepared for technology transfer into QC. This will be achieved by collaborating with the organization's subject matter experts on analytical methods and validation strategies that are scientifically sound, phase-appropriate, compliant with regulatory expectations, and executed consistently.
The successful candidate will be motivated by the opportunity to plan, execute, and lead impactful work to help advance life-changing iPSC-derived therapies from development towards patient administration and enable FCDI to deliver these therapies efficiently, safely, and with the highest standards of quality. This is an onsite role located at our sites in the Madison, WI area.
The Lead Associate 3, Quality Control (QC) Microbiology oversees and guides the critical operational functions of the QC Microbiology laboratory. This position holds the responsibility for conducting microbiological assays, as well as effectively trains junior analysts in these areas. The role is pivotal in guaranteeing “right the first time” execution to support timely batch disposition of manufacturing goods. Additionally, this role ensures technical issues are promptly escalated to laboratory management and upholds high standards of accuracy and efficiency within the laboratory operations.
Shift: Monday – Friday (8am – 5pm)
The Supervisor, QC Microbiology leads a team of microbiology analysts to execute GMP testing, environmental monitoring, and microbiological control programs supporting clinical and/or commercial manufacturing. This role ensures cGMP compliance, data integrity, safety, and right first-time performance, while driving method robustness, investigation quality, and continuous improvement. The Supervisor typically supervises staff and junior scientists, manages day-to-day operations, and contributes to cross functional initiatives of moderate complexity.
Shift: Wednesday – Saturday (7am – 5pm)
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