The Supervisor of Instrumentation & Controls (I&C) is responsible for overseeing and coordinating the operational reliability of the site instruments through an effective calibration process. This role focuses on maintaining and manages equipment, processes, and daily activities while ensuring compliance with safety, regulatory, and Good Manufacturing Practice (GMP) standards. Additionally, the Supervisor provides training, technical support, and leadership to the I&C team.

2nd Shift

Position Description

We are hiring a Executive Director, Site Leader. The Executive Director, Site Leader will provide site leadership to achieve the Company’s objectives related to research, development, and manufacturing of recombinant proteins and other biomolecules. The Site Leader serves as the primary interface with business / corporate leadership, regulatory authorities, and key partners, while building a high-performing, inclusive team that consistently achieves objectives

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 following:

Position Description

We are hiring a Distribution Market Development Manager. The Distribution Market Development Manager will support the Fujifilm Biosciences business strategy and execution. This role will implement the strategic direction from global marketing to build a distribution marketing plan.

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 QA Technical Specialist, QA for QC is responsible for partnering and helping drive Quality oversight for the direction of all QC Laboratory processes. The QA Technical Specialist, QA for QC collaborates with other project teams, and with QA departments to align strategies and procedures. The QA Technical Specialist, QA for QC continues to ensure that all QC Laboratory systems and processes are operated/maintained in a validated state throughout their lifecycle, with a focus on consistent policy administration, QA oversight of day-to-day activities and resolution or mitigation of issues occurring during operation.

This role provides essential quality assurance compliance review support for stability, drug product release, raw material release and Batch disposition. The role is also a primary quality assurance contact for QC deviations. Additionally, this role also supports Analytical Development (AD) group on method qualification document reviews and ensuring test method is effective in the system.

GENERAL PURPOSE

The Quality Control Technical Coordinator serves as the primary front-line support for a broad range of technical and administrative activities within the Quality Control Laboratory of the Ink Jet Printing Materials Business Unit at NCS. Acting as a critical liaison between management and laboratory technicians, the technical coordinator provides mentorship, supports daily operations, and ensures seamless execution of quality control processes to maintain excellence in product quality and laboratory performance.

ABOUT FUJIFILM

About the Global Business: Celebrating our 90-year anniversary in 2024, Japan’s pioneering photographic film maker, Fujifilm has leveraged its imaging and information technology to become a global presence known for innovation in healthcare, graphic arts, optical devices, highly functional materials and other high technology products. We use leading-edge, proprietary technologies to provide top-quality products and services that contribute to the advancement of culture, science, technology and industry, as well as improved health and environmental protection in society. Anchored by an open, fair and clear corporate culture and with leading-edge, proprietary technologies, Fujifilm is determined to remain a leading company by boldly taking up the challenge of developing new products and creating new value.

About FUJIFILM Ink Solutions Group: Comprised of 3 manufacturing sites FUJIFILM Ink Solutions Group, is an experienced inkjet technology partner to equipment manufacturers, integrators and ink formulators. We support our customers with full-service inkjet ink development and manufacturing, contract ink manufacturing services and supply of high quality pigment dispersion technology.  For over 50 years we have driven technology changes in screen, narrow web, textile and inkjet, building expertise across multiple market segments with a deep understanding of application and market requirements.

Our global team of six hundred experts in ink is supported by a network of dedicated technology development facilities and specialized manufacturing centers. Our infrastructure enables us to support projects of all sizes, including the largest OEMs and integrators with next generation machine developments for advanced applications, and we have the manufacturing capacity to meet the highest volume demands.

The Automation Engineer 3, BMS/VDS provides support for the sitewide Building Management System (BMS) and Validated Data System (VDS). This includes implementation of changes to the utility and facility automation systems, updating design documents, executing testing, troubleshooting events, and providing on-call support. This role participates in and may lead projects and medium- to complex-level changes while coordinating with internal and external stakeholders.

The Technician 3, HVAC/Refrigeration is responsible for the installation, maintenance, and repair of the heating, ventilation, air conditioning, and refrigeration systems/equipment. This role ensures these systems meet the stringent requirements of pharmaceutical manufacturing and storage environments. Additionally, this role is responsible for conducting regular inspections and preventative maintenance on HVAC/R systems to ensure they are operating within the required specifications.

The Utility Maintenance 3 performs corrective maintenance, routine maintenance, and preventive maintenance on plant utilities equipment following Standard Operating Procedures (SOPs), completes work orders, daily logs and forms following Good Manufacturing Practices (cGMP) documentation practices and quality standards in a Pharmaceutical Manufacturing plant. The corresponding utilities 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.

The Utility Maintenance 2 performs corrective maintenance, routine maintenance, and preventive maintenance on plant utilities equipment following Standard Operating Procedures (SOPs), completes work orders, daily logs and forms following Good Manufacturing Practices (cGMP) documentation practices and quality standards in a Pharmaceutical Manufacturing plant. The corresponding utilities 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.

The Automation Engineer MES provides 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. Additionally, this role participates in designing and maintain the Manufacturing Execution System (MES).

Openings available from entry-level to senior engineers. Join us and grow your automation career.

The Automation Engineer, 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.

Openings available from entry-level to senior engineers. Join us and grow your automation career.

The Automation Engineer, DSM Upstream, will provide support to the Drug Substance Manufacturing (DSM) facility using DeltaV. This includes implementing changes to the Automation systems, updating design documents, executing tests, troubleshooting events, and providing automation on-call support. This role focuses on supporting the delivery of DeltaV logic for Upstream process areas, including Inoculum Lab, Media Preparation, Seed Culture, Large Scale Bioreactors, and Harvest.

Openings available from entry-level to senior engineers. Join us and grow your automation career.

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 Carrollton, TX facility for a Manufacturing Technician!

With state-of-the-art manufacturing facilities in the U.S., Europe, Taiwan, China, Korea and Japan, local sales offices throughout the world and on-site applications support, FUJIFILM Electronic Materials supplies the world's top tier semiconductor manufacturers with a broad array of products and services used throughout the semiconductor manufacturing process.

The Role

Our Manufacturing Technicians fill a critical need in FUJIFILM's chemical plant operations. They support the daily operations in our fast-paced production area. As a Production Operator you will perform hands-on batch processing and liquid production of solvents. Loading and offloading of bulk chemical solvents and blends into tanker trucks, holding vessels, rail cars and drums. Monitor tank truck and rail car loading and unloading.

The CPQ, Medical Informatics (MI) Marketing Manager supports our CPQ market strategy and workflows for the Synapse Enterprise Imaging portfolio of products sold into the North America and Global markets. The CPQ MI Marketing Manager will assist in streamlining the quoting process of the portfolio, helping develop scalable quoting workflows, collaborating with product development, and supporting process improvements. The role involves supporting platform management and learning continuous improvement of quoting systems. The position works closely with our MI Marketing Operations team, product owners, sales leadership, finance, quality assurance, legal, and order management. The CPQ MI Marketing Manager should have a good understanding of the products within the Synapse enterprise imaging portfolio to assist in positioning the Guided Selling Strategies. This role requires collaboration with all members of the HCUS Medical Informatics organization and other cross-functional departments.

The Scientist 2, QC Analytical Development (AD) Chemistry 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, Holly Springs. 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 isoelectric focusing (icIEF)), wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc.

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 a Capital Planning Manager!

With state-of-the-art manufacturing facilities in the U.S., Europe, Taiwan, China, Korea and Japan, local sales offices throughout the world and on-site applications support, FUJIFILM Electronic Materials supplies the world's top tier semiconductor manufacturers with a broad array of products and services used throughout the semiconductor manufacturing process. 

The Role

The Capital Planning Manager leads the overall capital process. This position will have ownership of capital budget that is aligned with business and operational leaders to ensure that objectives that are consistent with business strategy are achieved in capital spending.

This position will partner with IT programmers to develop a capital approval and tracking process that streamlines the capital approvals and provides transparency on the status of capital approvals. The process will include management of the capital budget and a capital spending forecast. This position will monitor the health of the process using Key Performance Indicators with dashboards for regular reporting to stakeholders.

The manager will develop standardized project engineering tools, provide training in approach and execution, as well as develop specifications for standardization across the project engineering teams. The manager will also be a resource for project management as needed.

Our preference is for this position to be located at our Mesa, AZ facility but we could potentially consider the Pueblo, CO, Carrollton, TX or North Kingstown, RI metro areas for the right candidate.