Here are our current job openings that match your search criteria. Please click on the job title for additional information or to apply to the opening.
If you are a current employee, please use this link to apply via our Internal Application Portal.
Use the form below to perform another search.
The QA Engineer, Drug Substance Manufacturing (DSM) Operations is responsible to help drive the Quality oversight for the direction of all Drug Substance Manufacturing (DSM) processes through to operational readiness during project phase. This role is responsible for quality assurance oversight of day-to-day activities and resolution or mitigation of issues.
The Associate Manager, QA Pharmaceutical Quality Systems (PQS) supervises the PQS Document Management and Systems team for the enterprise Quality Systems administration and document control. Serving as the site Business Process Owner for quality system(s), this position is active in each system’s global advisory board and acts as primary point of contact for PQS. The role applies system expertise and business knowledge, gathers recommendations for system enhancements and gaps, prioritizes and implements solutions with leadership accordingly, maintains a deep understanding of the system(s) and process functionality/improvements, and understands such improvements’ local and global system(s) applications. The role also performs advanced system administration including but not limited to user management, user support, problem solving, and system training. The Associate Manager of PQS maintains relationships with site-based customers and global colleagues as well as provides updates to leadership as requested. Domestic and International travel is required.
The EHS Associate 2 role is a highly visible, trusted partner to Operations—present at the Gemba, quick to support, and committed to enabling safe, high-quality work. In this role, you will respond to day-to-day questions, assist with incident investigations, and risk assessments, support GEMBA walks and audits, and help teams integrate EHS into standard work. Your focus is to listen, coach, and collaborate so that every colleague can do their best work safely, every shift.
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.
Who We Are
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 for a Procore Administrator!
The Role
The Procore Administrator plays a vital role throughout the life of construction projects from startup to close out. This role works in conjunction with facilities, operations, and other key members to ensure projects have the most up to date documents, changes, and information. The Procure Administrator ensures the project is completed in a timely manner, with efficiency, and to FUJIFILM Electronic Materials (FFEM) standards.
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.
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 an Inventory Control Specialist!
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 Inventory Control Specialist is responsible for maintaining accurate inventory records and supporting inventory control activities for finished goods and raw materials at the Mesa, AZ warehouse. Using SAP and other inventory management tools, this position processes and verifies inventory transactions, performs cycle counts, manages inventory locations, and helps resolve discrepancies.
The position also supports warehouse operations by safely loading and unloading trucks and transporting materials using forklifts and other material-handling equipment.
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.
The Experience Design Team at Fujifilm Sonosite is looking for an exceptional Senior Visual Designer to envision, define, and design the future of visual medicine. The Senior Visual Designer is responsible for leading design projects and works within the design team and across all disciplines to deliver powerful, visually compelling solutions. Designers who fit at Fujifilm Sonosite have deep design chops, are passionate about delivering innovative solutions to medical professionals, and can demonstrate a track record collaborating across engineering, clinical and product management disciplines.
The Experience Design Team at Fujifilm Sonosite is looking for an exceptional Senior Industrial Designer to envision, define, and design the future of visual medicine. The Senior Industrial Designer is responsible for leading design projects and works within the design team and across all disciplines to deliver powerful, compelling solutions. Designers who fit at Fujifilm Sonosite have deep design chops, are passionate about delivering innovative solutions to medical professionals, and can demonstrate a track record collaborating across engineering, clinical and product management disciplines.
As the Inside Sales Representative, you will perform key functions as part of managing of the entire sales administration process. This telesales role is responsible for soliciting sales over the telephone and must possess marketing and sales acumen to develop leads. The position is responsible for generating leads, advancing the sales process, and transferring warm leads/new business through collaboration with the Sales team in support of overall goals and objectives. The Inside Sales Representative will research accounts and cultivate leads to reach business targets through telephone, email, or webinar. Also, acquires additional revenue based on regional needs.
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.
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 North Kingstown, RI facility for a Lab Technician to support 2nd shift operations!
The Role
Our Lab Technicians perform a wide range of functional testing on advanced, high purity chemical products used in Semiconductor manufacturing. This includes performing the required analytical/trace metal testing on a wide range of samples; in-process production samples from Formulation, Packaging and Research; packaged finished goods.
The successful candidate will assist in the evaluation of new test procedures including participation in gauge studies and monitor all instruments through Statistical Process Control.
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.
Software Powered by ICIMS
www.icims.com