We have an exciting opportunity at our North Kingstown, RI facility for a Senior Process Engineer!  The Senior Process Engineer will lead manufacturing engineering activities for batch-process-based product lines. This role involves full ownership of a product line while contributing to the success of additional lines. The Senior Engineer will oversee all aspects of the product lifecycle, ensuring quality standards for materials are maintained and committed ship dates for finished products are met. Responsibilities include evaluating supplier changes, developing qualification plans for validation, and implementing continuous improvement projects. The...

We have an exciting opportunity at our Hollister, CA facility for a Quality Control Engineer II!  The Quality Control Engineer II will work to ensure all metrology equipment provides a high level of quality that meets internal and external customer’s expectation. This individual will put in place a system to measure each critical metrology equipment performance, drive continuous improvements, and then report on its status with QC Chemists, Process Engineers, management, and key customers to address any deficiencies.

The Manufacturing Supervisor works as part of the Manufacturing team to deliver on goals to generate high quality materials that can be used both in the clinic as well as commercial.  This position will contribute to the successful delivery of released product in support of clinical trials and commercial requirements.  The Manufacturing Supervisor will work in different activities including manufacturing processes, facility cleaning, document review, inventory control and materials management.  The position will also provide manufacturing processing input for the design and operation of computer systems (MES, ERP, LIMS, QMS, EMS).  The candidate will also understand the...

We are hiring a Clinical Affairs Specialist. The Clinical Affairs Specialist will be responsible for assisting in the development and generation of Clinical Evaluation Plans and Reports (CEPs, CERs), conducting clinical literature searches, performing analysis of clinical literature, and evaluating and reviewing clinical data, generated both pre and post-market for medical devices and in vitro diagnostic devices. In addition, the Clinical Affairs Specialist will assist in performing annual...

The Microbiology IV will be responsible for the QC microbiological aspects of cGMP compliance and testing at the FUJIFILM Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory.  This position is a pivotal role to either a technical career path as a Microbiologist IV or a managerial career path as a Lead for the team, and a successful individual in this role will lead the team regardless of the career path they decide to pursue.  

The Quality Control Chemist II, with limited supervision, will be responsible for participating in the Technology Transfer of established methods into the FUJIFILM Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory.  Following Tech-Transfer Activities, the candidate will be responsible for performing release and stability testing using the established analytical methods.   Reports...

The Manager, QC Virology oversees the QC Virology team, ensuring GMP-compliant laboratory operations in accordance with regulatory guidelines. This role involves direct management of PCR, RT-PCR, qPCR assays, Adventitious Virus (AVA) testing, and Mouse Minute Virus (MMV) testing. As a technical subject matter expert, the Manager provides support for troubleshooting complex investigations and optimizing laboratory systems while ensuring accurate documentation and compliance with GMP standards. Additionally, this role represents the QC Virology team during customer and regulatory audits and foster the development of team members through effective leadership.

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.

We have an exciting opportunity for an SAP MII Developer!  The MII Developer will be responsible for managing projects and production support activities. Our ideal candidate should have 3+ years of experience with SAP MII Implementation / Designing Solutions / Development. The candidate must understand the internal working on SAP MII including but not limited to BLS, QT, Event Processing, and Alerting. Strong understanding of SAP NetWeaver is a must.

We have an exciting opportunity at our Mesa, Arizona facility for a Senior Research Chemist in our CMP group!  The Sr. Research Chemist will support new Chemical Mechanical Polishing/Planarization (CMP) slurry formulation development and provide chemistry/chemical component expert consultation to the technology development team. The primary focus will be formulation development for BEOL/MOL slurries for next generation semiconductor technologies.

We are hiring a Sr Manager, HRBP who will work a hybrid schedule out of our Valhalla, NY office.  Responsible for the management and delivery of core people and capability programs, including talent and performance management, year-end compensation planning and workforce planning within a business line.   Responsible for oversight of a facility and/or managing 1+ HR staff member(s).

We have an exciting opportunity at our Mesa, AZ facility for a Cyber Security Analyst!  The successful candidate will be responsible for assisting with the day-to-day operations of securing our various information systems. Reporting to the IT Infra/Security Manager, the CSA is tasked with providing technical expertise in all areas of network, system, and application security.

We have an exciting opportunity at our Mesa, AZ facility for an Applications Manager!  The successful candidate will be a vital leader in assisting businesses to achieve success, with responsibility for researching and acquiring the software applications required to propel growth forward. They will configure, monitor, and maintain these tools as needed, ensuring that they are used across departments. Furthermore, they are responsible for managing financial budgets associated with both projects and day-to-day operations, all while supervising server/hardware upgrades and reporting success to top management and stakeholders.

The Equipment Maintenance Technician III is responsible for the maintenance of wafer fabrication assembly and facilities equipment for production lines. Responsible for troubleshooting and repairing downed equipment and assisting engineering staff in establishing and implementing periodic equipment maintenance. Uses test and diagnostic equipment to perform checkouts. Rebuilds manufacturing equipment. Technician may participate in safety forums, Emergency Response Teams and station improvement teams.   -

The work we do at FDB has never been more important—and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. Join our new FDB facility in Thousand Oaks, CA and help manufacture the next cell therapy in partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion, energy and drive - what we call Genki.  The Manager Quality Control Analytical will manage a group of Quality Control activities at...

The Manufacturing Technician II work directly with a range of technologies. 

The QC Operations Manager will manage, maintain, and oversee the day-to-day operations of the Quality Control Coordinators, Sample Management, and Stability Coordinators.  The Quality Control Operations Manager will oversee and manage staff in a multi-functional support role.  This position will require the QC Operations Manager to supervise QC employees staffed in the following areas:  QC Project Coordinators, Sample Management, and Stability Coordinators. The position will also require frequent communication with the Analytical Development and Assay Method Transfer groups to coordinate and schedule method qualification activities.  The QC Operations...

The QC Supervisor, Cell Biology will be responsible for coordinating the installation and qualification of new analytical equipment in support of GMP release and stability testing.  The Cell Biology/Immunology Supervisor will lead tech transfer activities of qualified cell based and immunological methods from designated donor laboratories.  The Supervisor will play a pivotal role in selecting qualified personnel to staff the QC Cell Biology laboratory.   

We are seeking an IT professional with experience designing, developing, deploying and supporting manufacturing systems.  Experience with Manufacturing Execution Systems (MES), Enterprise Resource Planning (ERP) systems, and large Databases desired.  Experience with SAP ME, MII, ME SDK and PCo based solutions, as well as Oracle Database helpful.  The Manufacturing Systems Analyst III will work on Manufacturing and Business application configuration and support in a manufacturing environment.  

We are hiring a VP of Finance and Investor Relations as a remote position, prefer person based in the NY, NJ, or CT area.  The VP of Finance and Investor Relations is a key member of the FUJIFILM Holdings America Leadership team. This position will be responsible for overseeing all financial activities for the shared services organization and parent Company which supports 27 legal entities in the Americas. Leading key activities of strategic planning, financial forecasting, budgeting, investor relations, general accounting, tax, accounts payable and receivables as well as credit operations. The ideal candidate will have a very strong...