We are hiring for a Wall Décor Operator for the Imaging Division (ID) which provides consumer and commercial photographic products and services. The position is responsible for efficiently working with materials in the production area, while effectively operating and maintaining equipment with limited assistance. This position reports to the Production Supervisor in Greenwood, SC. 

The Associate Manager of Instrumentation & Controls (I&C) ensures the efficiency and operational reliability of the site instruments through an effective calibration process. This role sets the direction and manages the development of the I&C team as the site transitions from construction to operations. Additionally, this role assists with establishing efficient programs designed fit for future operations by utilizing current Good Manufacturing Practice (cGMP) / Good Laboratory Practice (GLP) knowledge, work scheduling, instrument calibration, repair, and troubleshooting. This role also provides day-to-day oversight and development of the I&C team. 

The Manager of Environment, Health & Safety (EHS) will lead EHS and sustainability programs at the New Castle facility, driving improved performance through implementing EHS programs, ensuring KPIs are met and investigating all incidents /near miss. The position will also be responsible to ensure all environmental and compliance requirements for the facility are met. The position is also responsible to lead the safety committee and delivering all relevant training for the employees.

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 FDB and help create the next vaccine, cure, or gene 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 FDB call Genki.

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

Summary:  The Validation Engineer II, under moderate supervision, will be responsible for drafting System Impact Assessments (SIAs), drafting and executing validation protocols for Facilities, Utilities, Systems and Equipment (FUSE), as well as preparing validation final reports for the same.

Summary: The Manufacturing Readiness Coordinator I assists the Manufacturing team to ensure right-first-time execution on the GMP manufacturing floor and on time starts by coordinating and delivering readiness milestones.

The Manager, QC Microbiology is responsible for contributing to key functional, tactical, and operational aspects of the QC group at Fujifilm  Biotechnologies. Project management, initiation of process improvements, liaison for, qualification and validation activities, modeling the leadership competencies, aiding in the development of peers and performing QC approval, as required. The Manager, QC Microbiology is proficient in their understanding of Quality Systems and applies that knowledge in leading projects, coaching, and continuous  improvements of systems cross-functionally.

Summary:  The Sample Management Analyst I, under general direction, will be responsible for performing routine and non-routine support of samples submitted to the Quality Control (QC) Laboratory for evaluation. This position works as part of the Sample Management team to manage the receipt, organization and inventory of samples from manufacturing, clients, other Fujifilm facilities and third parties. The Sample Management Analyst I arrange sample shipments for outsource testing and shipments to Clients or other facilities and controls dispensing of samples...

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

The Manufacturing Technician II works directly with a range of technologies. Dependent upon assignment, the range of technologies may include any of the following:

Senior Laboratory Engineering Technical Support Specialist is a senior-level position in the Laboratory Engineering department of FDBT. The primary purpose of this position is to provide day-to-day technical support for the analytical pcs and equipment within Manufacturing, Quality Control, Analytical and Process Development organizations. In addition, this position is a major contributor to supporting new technology and equipment life cycle monitoring.   Under minimal supervision, the Senior Laboratory Engineering...

Position Description - Manufacturing Quality Engineer II for FUJIFILM Dimatix, Inc, Lebanon, NH.   Design, implement, and maintain quality assurance protocols and methods for processing materials into partially finished or finished products. Plan, implement, and manage compliance of manufacturing and production processes with internal and external safety, quality and regulatory standards requirements for worldwide distribution. Design methods and procedures for inspecting, testing and evaluating the precision and accuracy of production...

The Supervisor, Manufacturing Support is responsible for leading the material, training and production scheduling teams within manufacturing support and their associated activities to ensure compliant and reliable production.

We have an opportunity for a dedicated team player to be a part of a fast-paced, busy manufacturing environment! Fujifilm, Sonosite, Inc is seeking Manufacturing Associates to join our team. This role has full benefits, a 401K plan, paid time off, plus more perks that come with being a full time Fujifilm Sonosite employee! As a successful candidate you will exhibit manual dexterity, reliability, basic math and computer skills and an aptitude for learning things quickly.    This position is responsible for performing a...

We have an opportunity for a dedicated team player to be a part of a fast-paced, busy manufacturing environment! Fujifilm, Sonosite, Inc is seeking Manufacturing Associates to join our team. This role has full benefits, a 401K plan, paid time off, plus more perks that come with being a full time Fujifilm Sonosite employee! As a successful candidate you will exhibit manual dexterity, reliability, basic math and computer skills and an aptitude for learning things quickly.    This position is responsible for performing a...

Manufacturing Associate (1st Shift, Transducers) - Bothell, WA   This position is responsible for performing a variety of tasks associated with manufacturing diagnostic ultrasound transducers.  Specific tasks may include some of the...

The Microbiologist I will be responsible for assisting the QC microbiological aspects of cGMP compliance and testing at the FUJIFILM Biotechnologies Texas Quality Control Laboratory.    Reports to                Supervisor, Microbiology

The I&C Engineer provides engineering support to field personnel in the performance of maintenance and operational tasks associated with instrumentation and automation systems and controls across the campus. The I&C Engineer provides support for the metrology department through evaluations of instrument deficiencies, test equipment issues and calibration strategies and methods. This role works directly with other Utility Engineers ensuring applicable safety and regulatory standards are maintained, identifies process improvements, and assists with troubleshooting equipment issues to maintain overall plant reliability. Additional responsibilities includes supporting deviation investigations and...

Utility Maintenance 2 will perform corrective maintenance, routine maintenance, and preventive maintenance on plant utilities equipment following Standard Operating Procedures (SOPs). Complete work orders, daily logs and forms following Good Manufacturing Practices (cGMP) documentation practices and quality standards in a Pharmaceutical Manufacturing plant. Utilities to include high-pressure steam boilers, process wastewater treatment, chillers, water purification systems (water softening and carbon bed filtration, reverse osmosis, deionization equipment, sanitary pumps, and associated equipment), compressed air and dryers, and chilled water