The Automation Engineer 3 will provide 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.

The Manufacturing Specialist 1 performs manufacturing support activities to ensure compliant and reliable production. This manufacturing facility will be 24/7 operational and the role may require to be flexible with working hours and shift rotation.   

This role leads a shift team and is responsible for manufacturing bulk drug substance. This manufacturing facility is 24/7 operational and the role may require to be flexible with working hours.

The Clinical Consultant, MI – I shall be responsible for providing clinical consulting for the project, report configuration (CV), workflow analysis, end-to-end testing, remote or onsite training as well as go-live support to Synapse PACS/MI projects. In addition, provide clinical support for sales and company team members with respect to the use of the company’s products and serve as a consultant on behalf of customers and company personnel in compliance with the company’s quality procedures. Assist with TAC Support.  

The QC Lead Associate II will support a broad range of analytical disciplines within the Quality Control laboratory. This position will perform testing focused on biochemistry plate and gel based-assays in the QC Analytical Chemistry laboratory. The individual performs high throughput, right-first-time laboratory work to meet production schedules and project milestones and will work with minimal supervision. They are expected to follow procedures and have familiarity and proficiency with a wide variety of analytical methods and supporting data management processes. The individual effectively and efficiently manages complex or difficult tasks. Analytical...

This position is intended to sell Fujifilm medical imaging devices, options, and service contracts to prospective and existing customers in their assigned territory, Arizon / Utah and Las Vegas locations. 

The Project Manager role provides project management and communications support for complex, critical projects related to the development and operation of a greenfield Biotech Manufacturing facility. The primary focus is on establishing and facilitating continuous improvement and risk management initiatives to ensure the new site is adequately prepared for both initial startup and ongoing operations. This position leads, facilitates and

We are hiring a Powder Milling & Cleaning Technician. The Powder Milling & Cleaning Technician will be responsible for the milling of powdered media and cleaning of powder media equipment.   Shift- 2nd- 1:00 pm-9:30 pm

We are hiring a Powder Formulation Technician. The Powder Formulation Technician will be responsible for the formulation of powder media.   First Shift: 5:00 am-1:30 pm

This position reports directly to the Senior Director of Marketing and has overall responsibility for instax™ product management and product marketing.    Accountable for executing annual strategies and overseeing instax™ product staff (2), supporting both internal teams and external stakeholders (sales/retail partners).   The Director of Product Management for instax™ is...

We have an exciting opportunity at our North Kingstown, RI facility for a Warehouse Technician!  The Warehouse Technician is responsible for shipping goods to customers and/or external warehouses and for providing materials and supplies to the manufacturing, laboratory, engineering and R&D groups for various activities. This is a 1st shift opportunity which will include shift differential pay in addition to our amazing benefits package!

The Senior Director, Media and External Relations role is part of the global Corporate Affairs team, supporting all of our sites around the globe. The role is essential in managing the company’s external communications and reputation, with a strong emphasis on building relationships with top-tier U.S. media outlets. You will be responsible for crafting and executing media strategies, monitoring media coverage, and creating content for our external channels. A key aspect of this role is collaborating with teams geographies Europe, US and Japan and functions such as finance, commercial, and investor relations, ensuring aligned messaging that resonates with key external...

The Director, Quality Systems and Support oversees and leads the QA Systems and Support function within FDBN. This includes, but is not limited to, managing team, ensuring the accuracy and timeliness of departmental deliverables, and upholding company core values. This role is also responsible for hosting and executing Quality site audits and regulatory inspections. Additionally, it supports QA Digital Technologies teams, Pharmaceutical Quality Systems, Application and Records Management, and Operational GMP Learning. This role ensures adherence to corporate policies and procedures for key quality subsystems (e.g., Business Process Owners for Change Management...

The Scientific Applications Specialist provides technical field support for existing and new products of VisualSonics and its ultra high frequency ultrasound and photoacoustic technology. The Applications Specialist role is to be a subject matter expert in preclinical ultrasound and photoacoustic imaging. They will demonstrate the value of VisualSonics products through successful sales demonstrations, customer education and training.   **This is a US based travel position; however, some international travel may be...

The Environmental, Health & Safety (EHS) Specialist supports and implements the company’s Safety, Environmental, and Health Programs to ensure compliance with local, state, and federal regulations, as well as corporate policies. This role fosters a culture of safety and environmental stewardship while driving proactive measures, continuous improvement, and supporting EHS initiatives in laboratory and biosafety settings.

We have an exciting opportunity at our Mesa, Arizona facility for a Manufacturing Technician in our CMP slurries group!  The Manufacturing Technician - CMP supports receiving and cleaning containers, monitoring distillations, and packaging containers.

The Manufacturing Associate works as part of the manufacturing team to deliver high quality cell therapy materials during process transfers, routine production, and technology improvements. This position contributes to the successful delivery of released product in support of clinical trials and commercial production.  

The QC Analytical Development (AD) Chemistry Scientist 2 is responsible for coordinating the transfer of analytical methods for Technology Transfer (TT) of drug substance (DS) and drug product (DP) into the Quality Control laboratories of FUJIFILM Biotechnologies Diosynth Holly Springs (FDBN). The QC AD Chemistry Scientist 2 ensures GMP compliant laboratory operations in accordance with regulatory guidelines. This role coordinates analytical method transfers from clients, including the following analytical methods: chromatography (GC, HPLC, UPLC, SEC), spectroscopy (MS, GC/MS, LC-MS/MS, UV, UV-Vis, FTIR), electrophoresis (GE, non-reducing and reducing CE-SDS, imaged capillary...

The QC AD Chemistry Sr. Analyst I works with limited direction to support the execution of analytical method transfers and validations for drug substance (DS) and drug product (DP) manufacturing into the Quality Control laboratories of FUJIFILM Biotechnologies Diosynth Holly Springs (FDBN). The analytical chemistry methods used in biological product manufacturing include chromatography, spectroscopy, electrophoresis, wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc. The QC AD Chemistry Sr. Analyst I adheres to GMP compliant laboratory operations in accordance with regulatory guidelines. This role executes analytical...

The Analytical Development (AD) Tech Transfer (TT) Scientist 2 manages and coordinates the transfer of drug substance and drug product QC analytical methods from customers into the large-scale manufacturing facility, from first campaign through commercialization (clinical through process performance qualification/commercial). This role interfaces with customers and cross-functional teams to scope analytical testing plans and achieve project milestones. This role authors/reviews transfer plans, method transfer documents, transfer summary reports and specification justification reports, as needed. This role effectively communicates and operates between different teams, ensuring...