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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 Senior Particle Chemist!
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
The Senior Particle Chemist will primarily focus on silica particle synthesis and surface modification, dedicating significant effort to developing and optimizing particle fabrication processes. This includes designing, synthesizing, and tailoring silica particles with precise control over size, morphology, and surface properties to meet stringent performance requirements. Additionally, the role involves leading the development of BEOL slurry and buff chemical formulations, driving innovation through fundamental and mechanistic studies to enhance formulation performance and reliability.
The candidate will apply deep scientific expertise to support emerging materials and next-generation technology development, solving complex challenges to ensure advanced CMP solutions align with evolving industry demands and contribute to the successful commercialization of cutting-edge semiconductor processes.
FUJIFILM Cellular Dynamics, Inc. is seeking an accomplished Controller to play a key role in strengthening our accounting rigor in support of informed business decisions. This position will develop and maintain accounting systems that enable accurate forecasting and reporting, while overseeing accounts receivable, accounts payable, inventory, and other transactional functions and team members.
The ideal candidate is a highly organized, detail-oriented accounting professional who brings rigor to accounting and financial processes, identifies opportunities for continuous improvement, and establishes efficient, reliable ways of working. As an accounting expert, the Controller will provide guidance to the finance and accounting team and collaborate with internal customers across various FUJIFILM business units through both direct and indirect reporting relationships.
Job Title: QA Supervisor – Regulatory Affairs
Worksite: Bryan, TX
Requisition # 2026-38809
Job Description: QA Supervisor – Regulatory Affairs for FUJIFILM Diosynth Biotechnologies Texas LLC, Bryan, TX. Responsible for supporting the electronic publishing of regulatory submissions for national and regional regulatory agencies, and FUJIFILM Diosynth partner companies with the primary focus on moderate to complex regulatory submissions in both eCTD and non-eCTD format. Supports all CMC regulatory affairs activities for FUJIFILM Diosynth partner companies’ products, summarize regulatory intelligence, provides CMC regulatory input for regulatory submissions, and manages the compilation and SME review of CMC sections of all submissions for completeness and quality.(25%). Specific job duties include the following: Obtain data/documents from multiple internal teams for exchange and/or communication with FUJIFILM Diosynth partner companies. Upload information to the Regulatory documentation management location for future use.(25%) May be required to compile and report key information to pertinent stakeholders within the Quality team to ensure proper visibility and communication. Support a vibrant regulatory culture, working among functional groups as a teammate and collaborator to develop successful regulatory strategies.(10%). Produce and manage the generation of documentation to be submitted to worldwide governmental regulatory agencies to secure approvals for marketing products manufactured and/or distributed by FUJIFILM Diosynth partners. (15%) Support development teams working towards modifying existing processes or creating new processes; ensure compliance with existing design controls, risk management, and domestic and international regulations.(5%) Ensure timely approvals, communicate, and support negotiations with the FDA and other regulatory bodies as needed to identify pre-submission requirements and strategy and to resolve post-submission queries and issues.(5%) Maintain proficiency on regulatory requirements; and FDA/Notified Body published reviews as applicable.(5%) Provide continuing regulatory education and disseminate regulatory information to the product development, marketing, and clinical groups. Ensure that regulatory intelligence communications are disseminated in a timely manner to the appropriate business functions. (5%) Be responsible for ensuring personal and Company compliance with all Federal, State local, and Company regulations, policies, and procedures. Support the review and negotiation of Master Service Agreements (MSA) and Quality Agreements (QAg).(5%)
Build the analytics backbone that powers smarter manufacturing. As FUJIFILM Biotechnologies' Senior System Engineer — MSAT Applications, you will own and evolve the platforms that let our Manufacturing Science & Technology (MSAT) teams see, understand, and control processes in real time. From SIMCA-online and TIBCO Statistica to PAT and historian integrations, you’ll make sure these GxP systems are secure, validated, reliable, and fast—so scientists and engineers can make data-driven decisions that improve yield, reduce deviations, and speed life-changing therapies to patients.
Help build reliable, compliant manufacturing from day one. As a Manufacturing Support Associate 3, Tech Transfer, you’ll be a hands-on process expert who leads operational readiness, drives troubleshooting, and keeps production running smoothly in a 24/7 facility—while upholding the highest standards of safety, quality, and documentation.
The Sr. Systems Engineer is a key contributor, providing leadership and expertise in driving new and sustaining engineering product deliverables through all development phases. The Sr. Systems Engineer will leverage quantitative approaches for design, system, and technology integration activities to demonstrate visible and measurable progress for successful delivery as defined within Fujifilm Sonosite’s Product Development Process (PDP) and in compliance with FDA CFR and ISO/IEC guidelines. The person in this position will participate in the leadership of R&D from within the cross-functional team that identifies opportunities, collaborates with external partners, develops and manages requirements, generates system architectures and component concepts, implements the solutions in hardware and software, analyzes data, and ensures robust verification and validation testing along with cost, risk, and lifecycle management.
General Summary
The Quality Assurance (QA) Specialist will be responsible for supporting the corporate wide engineering and quality mandates and will work closely with both Engineering and QAT (the Quality Assurance Test team). Key responsibilities include project testing activities, documentation of test cases, review of requirements and design documentation, execution of integration and validation test plans, creating and maintaining test tools/equipment, defect reporting and defect management, quality goal setting, and recommending process improvements.
Essential Job Functions:
Develop and maintain test procedures for the areas of new and existing functionality in the product(s).
Conduct testing in various phases including integration and validation, logging all defects. Executing the system test procedures.
Conduct ongoing integration and regression tests of the product.
Analyze test results and defect data to identify problematic products.
Maintain test procedures and test records for project release testing.
Advise any ideas for the improvement of the team or processes.
In a timely fashion, report any variances from the target completion date of the tasks, or that the tasks cannot be completed.
Create and maintain testing tools/equipment.
Work effectively in collaboration with staff across the organization.
Assist in providing training and support to other departments on Quality Manual and Procedures as required.
Produce quality reports as required.
Other duties as directed by System Verification Manager or Senior Management.
Knowledge/Experience:
Formal post-secondary degree/diploma in computer science, engineering or a related discipline is desirable
1-2 years experience working with ISO 9001 and ISO 13485 quality standards is desirable.
1-2 years experience in development and execution of test plans in a development environment.
Experience working (as an intern or full-time employee) for a commercial diagnostic ultrasound company
Working experience in a clinical environment is an asset.
Experience with all aspects of the development lifecycle.
Skills/Abilities:
Thorough understanding of test methodology, including test plans, system and integration level testing, and status reporting.
Understanding of Quality Assurance methods.
Ability to plan and execute testing activities and projects
Familiarity with Microsoft family of products (Word / Excel).
Familiarity with C# or equivalent languages is an asset.
Familiarity with defect tracking software packages.
Ability to quickly understand and then utilize new software packages.
Excellent oral and written communication skills.
Detail orientated when learning and testing.
Ability to work independently as well as participate in a team of professionals.
Ability to respond to urgent situations appropriately by prioritization.
Ability to leverage relationships across other departments.
Ability to follow up with individuals without guidance.
Ability to adapt to project timelines and changes to priorities.
Accuracy and strong attention to detail is essential.
Willingness to learn.
Disclaimer:
The above information on this job description and specification has been designed to indicate the general nature and level of work performed by employees within this job. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.
The Continuous Improvement Director will lead operational excellence programs for FUJIFILM Cellular Dynamics, Inc. (FCDI), designing the FCDI continuous improvement system, and building a culture of continuous improvement. This role will own continuous improvement transformation by identifying opportunities and driving solutions which bring cost savings, efficiency gains, and improved quality. This role will create and sustain an operating system that drives a continuous improvement mindset at all levels and in all functions.
Senior Employee Relations Partner is critical in supporting managers and leaders to maintain a fair, harmonious workplace that supports organizational goals. Senior ER Partner will have current employment law knowledge and will manage and deliver a caseload of employee relations cases. In addition to upskilling managers on the management of cases and support on avoiding conduct issues. The Senior ER Partner is an experienced professional who requires minimal supervision or support.
As the Production Manager you will be responsible for carrying out day to day activities in multiple areas including production, inventory management, and quality investigations. Responsible to meet production throughput, quality, and cost objectives while driving waste from the process. Manages and develops one or more team leads as well as other direct labor staff. Also the job responsibilities may require off shift or weekend support. In this role you will be challenged to manage our Ultrasound Production Lines and its related processes and staff to deliver products with the highest quality at the lowest cost, according to product specifications and compliance requirements. Your team will consist of Assemblers, Test Technicians and Material Handlers across 2 shifts, Key Performance Indicators include On-Time Shipments, Defect per unit, Cost Reductions, Team Productivity, Safety, and more.
The QA Engineer, Validation is responsible for helping to drive the Quality oversight for commissioning and qualification processes. This role is responsible for quality assurance oversight, review, and approval of validation activities and documents associated with new systems, changes to existing systems, maintaining the validated state of equipment/processes/systems, and decommissioning.
The QA Specialist, DSM Operations (Days 2-2-3 0600-1800) is responsible for partnering in the Quality oversight of Drug Substance Manufacturing processes. This role provides oversight of validation program execution for these processes and systems to ensure applicable DSM systems and processes are operated/maintained in a validated state throughout their lifecycle, with a focus on consistent policy administration. The QA Specialist, DSM Operations ensures QA oversight of day-to-day activities and resolution or mitigation of issues occurring during operation.
Territory Manager - Houston, TX - Remote
As a member of our sales team, you will sell portable ultrasound systems in a consultative, professional and high velocity sales environment. This includes creating primary market demand for FUJIFILM Sonosite products by networking, cold calling, and educating users in hospitals and the physician office market on the value of FUJIFILM Sonosite’s hand-carried compact ultrasound systems and tools.
This position requires previous medical equipment sales experience.
To best serve the territory, prefer candidates currently located in the Houston, TX area.
This position is within the Imaging Division (ID) and provides consumer and commercial photographic products and services. This position is responsible for leading a team of 12 direct reports. (Quality Control Technicians, Inventory Control Coordinator, Maintenance Technicians) The Technical Maintenance Supervisor is responsible for efficiently working as a member of leadership driving the values by transforming the Technical Maintenance Team into a customer-focused, proactive operation that will help drive Fujifilm’s business. This position reports to the Operation Manager in Greenwood, SC.
We are seeking a Facility Mechanic II. This role performs general to intermediate facility repairs/cosmetic improvements to plant facilities. Performs routine mechanical troubleshooting and preventive maintenance (PM) tasks.
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 Manufacturing Technician within our Packaging group!
The Role
This role performs critical tasks such as drum and tote preparation, rinse, fill, material handling, and sampling duties.
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 Process Operator in our Acids group!
The Role
The Process Operator performs bulk unloading for 70% HF, Phos, Nitric and Acetic. Resposabilities also include compounding of blend tanks including pilot plant operations in support of our R&D group, passivation of new containers, processing secondary market materials and packaging sampling of incoming raw materials and finished product.
*This position is onsite in New Castle DE
Job Purpose
Support and optimize materials management and production planning by managing inventory, maintaining accurate SAP data, coordinating supply chain activities, and helping to align production schedules with customer demand. This role ensures the efficient flow of materials and information across the supply chain, helps to drive continuous improvement initiatives, and meet business objectives related to cost, quality, service levels, and regulatory compliance.
About Fujifilm
Global Business
Fujifilm, celebrating 90 years of innovation in healthcare, graphic arts, optical devices, and high technology products in 2024, leverages proprietary technologies to enhance culture, science, industry, health, and environmental protection. Our corporate culture promotes openness, fairness, and clarity.
Fujifilm Ink Solutions Group
With over 50 years of expertise and a global team of 600 professionals, we provide full-service inkjet ink development and manufacturing. Our facilities in the UK, USA, and India support projects from small to large scales.
The Warehouse Operations Coordinator is responsible for overseeing the efficient operation of the warehouse, ensuring that all shipping, receiving, and inventory processes run smoothly. This role involves managing a team of warehouse staff, maintaining safety and security protocols, monitoring key performance indicators (KPIs), and ensuring that daily workflow aligns with company objectives.
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