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Job purpose
The Associate Clinical Specialist independently provides customer support of Fujifilm’s ES equipment in the Endoscopy department and/or specified departments. This role manages all relevant equipment and uses its own judgement and decision-making skills to provide troubleshooting and training for the proper handling of our equipment. This position provides on-site, hands-on client support for Fujifilm Endoscopy’s entire product catalog for assigned customers. It serves as the primary clinical resource for the Company and its sales team regionally and handles all related inquiries and issues. The ACS partners with and provides
training to all members of the customer’s staff, including physicians, reprocessing department, technicians, and nurses to independently manage and maintain customers’ Fujifilm equipment. Furthermore, it provides service to additional customers within the zone as required. This position reports directly to the Zone Sales Director or Regional Manager.
Position Description
We are hiring a Product Specialist II. The Product Specialist II will support custom business function for on-boarding new products and/or new site qualification. They will manage the qualification of new raw materials such as new chemicals and/or packaging, customer new site qualification and process new stability study requests.
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.
Job Title: Quality Assurance Specialist III
Employer: FUJIFILM Diosynth Biotechnologies Texas, LLC
Position Description:
Quality Assurance Specialist III for FUJIFILM Diosynth Biotechnologies Texas, LLC. Responsible for the review and approval of Quality System Records (e.g. Deviations/CAPAs/Complaints) and will handle all associated responsibilities in compliance with Fujifilm quality policies and site SOPs to ensure regulatory compliance. Assist with the tracking and coordination and remediation and closing of Deviations/CAPAs/Complaints. Responsible for daily metrics pertaining to pending deviations, CAPAs, customer & client complaints to ensure on time closures. Perform deviation, CAPA, customer complaint quality oversight and write up of client complaints to ensure root cause analysis and write up of investigation are clear and concise. Conduct timely information gathering sessions with cross-functional departments to obtain the required information and data to complete the review and closure of investigations. Support client due diligence and Quality audits as well as regulatory inspections. Work with Quality management to implement and grow phase-appropriate quality systems that will enable cGMP manufacturing of pre-clinical to commercial products. Support client audit requests. Ensure self, and team, have no overdue training, or site actions. Support other QA teams and other functions in completion of site actions. Provide cGMP assistance with cross-functional departments, such as Facilities, Materials Management, Quality Assurance and Validation. Promptly notify Senior Management of potential quality or regulatory issues that may affect product quality or regulatory compliance.
This position is intended to provide Complaint Handling support to FUJIFILM Healthcare Americas Corporation. This position supports full, ongoing compliance to all applicable U.S. Food and Drug Administration (U.S. FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all other applicable laws, regulations, and standards.
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
The Product Manager will develop and support new and existing business of the CMP product lines. They will work closely with and take direction from the business management team. The key measures for success will be increased sales and profitability from existing and new product sales. Position will require in-depth knowledge of the semiconductor market, including key product characteristics, customer requirements, Fujifilm’s product implementation and support strategies, and relationships with key members at customer accounts.
The Analytical Project Leader serves as the single technical voice to the sponsor for their assigned early-stage programs. Each APL typically manages active programs under sponsor-batched governance.
The Process Engineer 2 that supports Drug Product Finished Goods (DPFG) within the assigned area(s) [Visual Inspection] provides engineering guidance to stakeholders throughout the organization to support capital projects, technology transfer, and manufacturing operations while ensuring processes are efficient, scalable, compliant with Current Good Manufacturing Practice (CGMP) regulations. This role adheres to product and customer requirements and works toward optimizing plant efficiency and reliability. This role also utilizes their experience with automated systems related to inspection of pharmaceutical products and camera and vision-based inspection systems.
The Account Executive, ES (Territory - KY, Southern Indiana, & Cincinnati) is responsible for the generation of sales revenue for the organization through personal interaction with prospective customers within a given territory. This position is expected to promote the use of core products within prospective customer accounts, maintain current customer accounts to ensure a solid reference base and educate the general market on the benefits of the product. This position must establish a solid network of reference with “partner” representatives who supply the same customers with non-competitive products and maintain a thorough understanding of competitive products and competitive positioning to ensure success and become a true “Endoscopic Consultant” for the customer. Has overall responsibility in achieving a 10% annual increase of market share.
The Maintenance Technician will report to the Maintenance Manager at QuickSnap in Greenwood, SC. The position is responsible for performing entry level to complex troubleshooting and repair techniques on manufacturing equipment; electrical/electronic and mechanical systems; analyzing, troubleshooting, maintaining, and repairing complex equipment; assisting in modifications to existing machinery and equipment to facilitate new production techniques and/or improve equipment reliability.
FNAC-ID 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 high-quality standards Fujifilm requires. Operations include molding, assembly, packaging, and shipping of QuickSnap cameras. QuickSnap operations also include recycling of spent cameras, in which 60% of the camera weight is reused to make new cameras.
Training on 1st shift: 7a-4:30pm Monday through Thursday. Friday 1/2 day 7am-11am.
Must take on call 1 day a week 5pm-5am. Training will be 6 months to 1 year.
Following training, this position will have a rotating schedule.
The Clinical Education & Product Coordination, Associate Regional independently provides in
person customer support of Fujifilm’s Endoscopy equipment during Fujifilm supported hands on
courses and/or training which primarily occurs on the weekend. This role serves as the primary
regional resource in managing requests for Fujifilm Endoscopy technologies for hands on courses
and trainings. This position manages all relevant equipment onsite, uses independent judgement
and decision-making to provide troubleshooting and training for the use and proper handling of
our equipment during events, and provides service and support to customers within the region as
required. This position reports directly to the Senior Manager, Clinical Education and Product
Coordination.
The QA Specialist, 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.
Position Description
We are hiring a Sr Scientist II. The Sr. Scientist II will be responsible for all activities relating to new product development, technical product support and applications, and process development.
The ideal candidate will have CHO and HEK experience as well as Stirred Tank bioreactor.
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 will operate the ammonium fluoride reactor processes, the nitric and hydrofluoric acid distillations, proprietary reactor process, and various utility processes, including the industrial waste treatment facility, deionized water facility and other support facilities. This individual will perform other process department duties and tasks as assigned. This person will also be a trained member of the Medical and Chemical Emergency Response and Confined Space rescue teams.
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 an Engineering Manager for our CMP group!
The Role
The CMP Process Engineering Manager is responsible for assuring that the work conducted by the customer-facing Process Engineering team is managed and adjusted, as needed to consistently meet the Manufacturing team’s commitments to CMP Product Management, the CMP Commercial Team, and our external customers.
The Process Engineering Manager is also responsible for assuring that workloads within the team stay properly balanced, that internal skill sets are properly matched to needs, and that professional development plans are created to ensure that additional skill sets are created as needed to meet changing internal and external requirements.
The Automation Engineer 3, DSM PI Data Historian, will provide Engineering input on the design, implementation, configuration, and testing qualification of the hardware for an Emerson DeltaV control system. Once in Operations, you will be responsible for and have ownership of the ongoing support of the control system hardware, software, and infrastructure.
The Sr. Manufacturing Manager manages and implements activities in the Print head manufacturing production areas to meet all production goals, quality goals, and cost objectives. The position is located onsite in our Lebanon, NH manufacturing facitility. Plans and prioritizes against production schedules for the 1st, 2nd and 3rd shift manufacturing operations based on anticipated demand, equipment efficiency, and materials supply. Plans, administers and assures production process procedures are in place and followed . This role will coordinate activities, as required, with other Operating groups. Other duties include making budgetary recommendations regarding expenditures and direct/indirect labor. Develops schedules and manpower requirements for assigned areas and selects, develops, and evaluates personnel to ensure the efficient operation of the function.
The Supply Chain Coordinator II develops and maintains integrated production planning and scheduling that encompasses materials to ensure that supply targets are met. This position is responsible for ordering and buying materials as well as tracking production and material consumption in the applicable system and tools.
Position Description
We are hiring a Director Data, AI and Analytics. The Director Data, AI and Analytics will own the strategy, platforms, operating model, and outcomes for Data, AI, and Analytics across three FUJIFILM life‑sciences businesses. In highly regulated GxP environments, deliver a trusted data backbone, governed self‑service analytics, advanced analytics, bioinformatics pipelines, and agentic AI—meeting 21 CFR Part 11/EU Annex 11, ALCOA+, and CSV/CSA expectations. Lead a cross‑site team (CoE + domain squads), partner with QA/CSV, Security, Lab IT, M&Q Systems, and ERP, and convert data and AI into measurable business value.
This position is hybrid in Irvine, CA.
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