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

POSITION SUMMARY: Develops, implements and maintains factory systems using C#, MS SQL Server, Eyelit MES and other custom products. Participates in cross-functional linked teams and vendors to design, architect and implement factory automation solutions.   Knowledge: Implementing software solutions for manufacturing process, preferably Semiconductor or Hard drive. Works on problems of moderate scope where analysis of situations or data requires a review of a variety...

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, AZ facility for a Manufacturing Technician within our Packaging group!  

The QA Project Manager, Program Quality Assurance (PQA) is responsible for providing the PQA team with assistance and oversight of QA projects. As projects evolve and startup activities develop, this position adapts its responsibilities to meet changing needs. The QA Project Manager, PQA focuses on establishing, facilitating, and delivering key performance indicators (KPI), continuous improvement and risk management activities in support of site readiness for operations, start-up and ongoing operations. This role is responsible for administering policies, and effectively addressing and mitigating any issues encountered during assigned activities. 

The QA Engineer, DSM Operations is responsible to help drive the Quality oversight for the direction of all Drug Substance Manufacturing (DSM) processes through to operational readiness during project phase. This role is responsible for quality assurance oversight of day-to-day activities and resolution or mitigation of issues. This role works 12-hour day shift on a 2-2-3 cadence, 0600-1800.

The Scientist 2, QC Microbiology, Drug Product & Raw Materials supports a broad range of microbiological functions for both raw materials and drug product manufacturing support. This role manages multiple assignments of increasing complexity and responsibility within the Quality Control laboratory in support of these two areas. This role follows procedures and has mastery of a wide variety of microbiological methods specific to raw material and drug...

About the Role   The Sr. Specialist 2, QC Program Management Technical transfer (TT) and Sample Support (SS) provides technical support through effective project management of the QC Sample Plans and QC Specifications in close collaboration with relevant stakeholders, including customers. The Sr Specialist 2, TT/SS interfaces with customers to scope QC Sample Plans and QC Specifications. This role participates in and leads collaborations with cross-functional teams as a representative of QC. This role supports the timely completion of...

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

The manufacturing associate in Drug Product Manufacturing will have a primary task for operation of filling line including all tasks related. This role will also support projects which influence manufacturing processes for DPM including training of others.  This position will also support and assist in scheduling daily manufacturing activities for the team. This manufacturing facility will be 24/7 operational and the role may require to be flexible with working hours or shift rotation.  

This role will lead and execute manufacturing processing steps, associated activities, and assist the supervisor as required. This position will ensure drug product manufacturing start up phase is supported from a knowledge standpoint and will then help the supervisor lead the manufacturing effort after start up phase.

The Associate Director, Data Integration and Reporting leads and drives the manufacturing data architecture design for the global implementation at FUJIFILM Biotechnologies. This role also leads the system life cycle activities for the global implementation of manufacturing data systems, such as historians, and reporting and integration platforms. This role continues to develop as the organization evolves.

The Associate Director, Digital Manufacturing leads and drives the Recipe Driven Operation (RDO) design for the global implementation at FUJIFILM Biotechnologies. This role also leads the global technology transfer activities and standards definition as they relate to Automation while defining and supporting the governance for life cycle of RDO and Configuration Environment for Batch Activities (CEBA). This role continues to develop as the organization evolves.

The Manufacturing Associate 2 executes and documents manufacturing processing activities per cGMP environment.. This manufacturing facility is 24/7 operational and the role may require to be flexible with working hours.

Summary:  The Finance Business Partner is a pivotal role within the Finance Function, primarily supporting the Associate Director of Financial Planning & Analysis in executing strategic initiatives for the site Finance organization. This position demands a high level of expertise in finance and project management, with a focus on driving efficiency and success in alignment with organizational...

Summary:  The Senior Accountant is responsible for overseeing the accounting, reporting and analysis of FUJIFILM Biotechnologies in TX accounting functions.  Responsibilities will include fixed assets as a primary function as well as month end close, data analysis, and operational accounting. This role requires to be highly organized, with a solid technical accounting knowledge base and excellent...

Summary:  The Computer System Validation (CSV) Engineer II, under general direction, will be responsible for drafting and executing validation protocols for computer systems, process control systems, as well as preparing validation final reports and all applicable lifecycle documentation.

This role performs manufacturing support activities to ensure compliant and reliable production. This manufacturing facility is 24/7 operational and the role may require to be flexible with working hours.   

Position Description We are hiring a MSS Manufacturing Supervisor. The MSS Manufacturing Supervisor will be responsible for all departmental production activities for manufacture of non-GMP products in the EMS Plant. They will act as a working supervisor performing manufacturing tasks as well as providing leadership to the manufacturing team.

Territory Manager - Hartford - Remote   As a member of our sales team, you will sell portable ultrasound systems in a consultative, professional and high velocity sales environment.  This includes creating primary market demand for FUJIFILM Sonosite products by networking, cold calling, and educating users in hospitals and the physician office...

The Automation Engineer 3, DSM Downstream 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. This role focuses on supporting the delivery of DeltaV logic for Downstream process areas including Buffer Preparation/Hold, Purification – Chromatography (LPC), Viral Filtration (VF), Ultrafiltration (UF), Diafiltration (DF), and Dispensing.