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The Supervisor, QC Chemistry, first shift is responsible for day-to-day supervision, audit readiness, and planning activities for the Chemistry laboratory. This Supervisor will lead a team responsible for performing routine testing of QC analytical chemistry methods used in biological product manufacturing, including chromatography, spectroscopy, electrophoresis, wet chemistry, glycan analysis, peptide mapping, and physical appearance.
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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 Carrolton, TX facility for a Warehouse Technician!
The Role
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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.
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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 Process Engineer to support our CMP Slurry operations!
The Role
Our Process Engineers provide the technical support to design, develop, troubleshoot,...
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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 Receptionist!
The Role
This role is a hybrid HR Administrator and Receptionist position. It will...
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Lead the launch of a world-class, 24/7 drug product manufacturing operation. As Associate Director, Drug Product Manufacturing, you will build and lead a new organization to achieve GMP readiness, onboard customers, and drive operational excellence across formulation, aseptic filling, wash and sterilization, inspection, and support. If you thrive on creating high-performing teams, shaping culture, and delivering results in a dynamic environment, this role is for you.
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A Sr Process Engineer 1 provides engineering technical guidance with limited or no direction, primarily focusing on client process fit within existing facility designs and specifying equipment and facility gaps for Drug Substance (DS) and Drug Product (DP) processes. This role champions transformation of engineering, manufacturing, and facility technologies, participates in industry forums, and provides technical engineering expertise for new processing equipment designs, installations and modifications to existing equipment and facility.
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Help bring life-changing medicines to patients by ensuring reliable, compliant manufacturing. As a Manufacturing Specialist I, DP, you’ll be a hands-on problem solver and process SME who keeps operations running smoothly in a 24/7 environment—driving documentation excellence, tech transfer readiness, and continuous improvement across Drug Product Finished Goods.
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The Automation Engineer 2, MES provides support to the Drug Substance Manufacturing (DSM) facility. This includes implementation of changes to the Automation systems, updating design documents, executing testing, troubleshooting events, and being a part of Automation on-call support. Additionally, this role participates in designing and maintain the Manufacturing Execution System (MES).
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GENERAL PURPOSE
The primary purpose of this position is to manufacture RxD dispersions at the COUS site.
The Production Operator must be responsible to perform all manufacturing activities
within all EHS, quality, and corporate guidelines on a right-first-time basis. The operator
is independently responsible for manufacturing activities and priorities, following all
appropriate training programs, complying with all documentation within the department
(i.e. SOP’s, process logs), and effectively communicating with other operators as well as
supervision and other departments. In addition, the Production Operator will...
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The Senior Specialist II, QC LIMS is a site-level and cross-functional leader for the Laboratory Information Management System (LIMS), operating with minimal oversight and in accordance with applicable regulatory, corporate, and scientific standards. This role architects, configures, validates, and governs the LIMS platform; plans and executes complex change initiatives; establishes and monitors system health and data integrity controls; and leads continuous improvement and...
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The Digital Design Specialist supports Computer Aided Design (CAD) and Building Information Modeling (BIM) technologies by leading the conversion,
governance, and quality of P&IDs and 3D models across operations and capital projects within a Good Manufacturing Practice (GMP) regulated facility.
This role operates autonomously, applying advanced problem-solving to complex models, data and standards while influencing stakeholders with varying
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We are hiring for a Manufacturing Technician. This position reports to Production Supervisor at QuickSnap in Greenwood, SC. Responsible for operating, cleaning, and general maintenance of the Quicksnap production lines.
Fujifilm QuickSnap Manufacturing produces QuickSnap one-time flash cameras as well as waterproof one-time use cameras. These cameras are made for the worldwide retail market to the...
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The Operations Program Coordinator is responsible for coordinating operational activities that support commercial and government accounts, including pricing updates, workflow tracking, documentation management, and cross-functional follow-up. Partners with internal teams to maintain accurate records, support implementation readiness, ensure timely completion of required tasks and milestones, and uphold the quality, accuracy, and completeness of data within Salesforce CRM.
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Help us connect strategy to outcomes. FUJIFILM Biotechnologies is hiring a Principal IT Business Relationship Partner (BRP) to serve as the primary liaison between Global IT and our site/business leaders. You will translate business priorities into actionable IT roadmaps, shape portfolio decisions, and guide delivery—elevating service reliability, compliance, and user experience in a regulated biopharma environment.
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Make a measurable impact on patient health by leading a high-performing team in a 24/7, state-of-the-art drug product facility. If you thrive on building people, solving problems, and delivering safe, high-quality products, this role is for you.
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The Weigh and Dispense Associate III is primarily responsible for the preparation and kitting of consumable and raw materials for cGMP process execution in Manufacturing. This role involves interaction with Quality, Manufacturing, Warehouse, Supply Planning, and Asset Planning to ensure successful operations. Responsibilities include weighing and dispensing materials, delivering goods to manufacturing, and handling return reconciliation when necessary. The Associate is required to work standard business hours, with potential for on-call duties and emergency response to maintain operational success.
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Job Title: Quality Assurance Specialist III
Employer: FUJIFILM Diosynth Biotechnologies Texas, LLC
Position Description:
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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, Arizona facility for a Product Manager!
The Role
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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 at our Mesa, Arizona facility for a Metrology R&D Chemist!