The Principal IT/OT Infrastructure and Security Architect will lead the creation and maintenance of the IT/OT roadmaps, and joint strategies for the mission critical infrastructure, this will be based on global alignment with all relevant stakeholders. They with drive the cybersecurity capabilities and roadmaps globally across IT and OT and ensure alignment with established standards such as NIST 800-82, ISA/IEC62443, CIS-20, and ISO27001. 

The Scientist 1, 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 product manufacturing and supporting data management processes. The Scientist 1, QC Microbiology (DP and RM) effectively and efficiently manages complex or difficult tasks with expertise within the assigned disciplines. This role initially supports the commissioning activities involved in the construction of a new Biopharmaceutical manufacturing facility and laboratory. Flexibility in job roles and assignments are required.

As the SIP/AI Integration Engineer III, you will take on leadership roles in software development to drive our front-end initiatives and full stack capabilities. You'll be a critical part of a dynamic team that integrates design and functionality, bringing products from concept to production with a mercenary-like initiative. This role is suited for someone who is passionate about creating seamless user experiences and building robust, scalable systems. The candidate will ensure timely test and integration of delivered software as hosted within state-of-art portable ultrasound devices.

The Quality Assurance - Compliance Specialist II - Audit and Inspection will support all associated responsibilities in compliance with FUJIFILM Diosynth Biotechnologies quality policies and site SOPs to ensure regulatory compliance. 

As a Strategic Sourcing Buyer, you will be responsible for leading and managing strategic sourcing activities for indirect spend categories throughout the contract life cycle. Collaborates closely with internal stakeholders across the Fujifilm Group Companies, including cross-functional teams and senior management, to align sourcing initiatives with business requirements. Develop and sustain supplier relationships through regular contact and operational reviews with key suppliers and partners. Responsible for the timely and cost-effective acquisition of assigned goods and/or services valued at $100,000 and greater, in accordance with corporate policies/procedures, best practices and federal acquisition regulations. 

This position is remote, but needs to be within a commutable distance to Greenwood, SC area. 

FUJIFILM Holdings America Corporation is the holding company for North American based FUJIFILM companies operating in many states across the US, as well as in Canada, Brazil and Colombia and engaged in the research, development, manufacture, sale and service of FUJIFILM products. The company serves a broad spectrum of industries in the U.S. including medical and life sciences, electronic, chemical, graphic arts, information systems, broadcast, and photography.

We are hiring for a Maintenance Technician Level 1 role. This position is within the Imaging Division (ID) and provides consumer and commercial photographic products and services. The position is responsible for troubleshooting and repairing all production equipment safely and timely for the manufacturing of Personalized Photo products. The job title Maintenance Technician Level 1 will report to the Maintenance Supervisor in Greenwood, SC.

FNAC-ID Personalized Photo Products Group (PPPG) now makes more than 450 personalized items (such as coffee mugs, posters, framed prints, canvas wall décor and more). PPPG provides a turnkey, back-end service of producing these items for a variety of retail and online customers. 

The Weigh and Dispense Associate position is responsible with assisting and executing in the set-up, and weighing of raw materials, solvents, and solutions used in GMP manufacturing at FDBN. This role will interact with manufacturing personnel in both Drug Substance and Drug Product teams as well as Warehouse for commercial operations and tech transfer activities required from the Weigh and Dispense operations. This role will be responsible for weighing and dispensing in operations, plus duties to deliver goods to manufacturing, as needed.

Additionally, there will be interim responsibilities associated with a large greenfield start-up, including international travel, performing system user acceptance testing, and setting up the dispensary area for GMP operations.

The Warehouse Associate 2 position is responsible for storage, handling, and distribution of materials and products. This role supports Warehouse operations in receiving, shipping, and/or logistics throughout FDBN and works with multiple functions to support operations (e.g., Manufacturing, Quality, Process Sciences), The Warehouse Associate 2 uses Systems Applications and Products (SAP) ERP system for inventory management, cycle counting, and shipping activities while operating in a good manufacturing practice (GMP) facility with standard operating procedures (SOPs).

Standard work hours for this position are 10AM-6:30PM ET. You may also be subject to shift work in the future.

Summary:  Reporting to the Director of Engineering, the Sr. Process Engineer at Fujifilm Diosynth Biotechnology Texas (FDBT) oversees engineering activities, including equipment installation and product introduction support, infrastructure assessments, and troubleshooting for process equipment and site utilities. The role involves supporting a range of equipment such as bioreactors, incubators, filtrations systems, and others. The engineer collaborates with various teams—facilities, manufacturing, CAPEX, validation, QA/QC, and contractors—for project implementation and equipment maintenance. Key responsibilities include driving process improvements via Change Control procedures and CAPA systems, supporting P&ID, maintenance strategy, SOP development, and equipment commissioning/qualification. Additionally, they lead equipment selection, sizing, material specification, utility needs, and URS development for future projects.

This position is intended to process all outgoing shipments, incoming purchase orders, incoming goods, schedule and process parts for repair, maintain the order and the neatness of the warehouse, assist in the physical counts of inventory, respond to off-hours emergency parts requests, and perform all other duties as assigned.

This position is intended to process all outgoing shipments, incoming purchase orders, incoming goods, schedule and process parts for repair, maintain the order and the neatness of the warehouse, assist in the physical counts of inventory, respond to off-hours emergency parts requests, and perform all other duties as assigned.

Are you a procurement enthusiast eager to make a difference in a company that will multiply its revenue and spend over the next five years? Would you like to help making medicine accessible to two billion people worldwide who do not have sufficient access today? 

Join our team as a Sourcing & Category Manager and be a part of something big! We're managing the company’s global and rapidly growing raw material spend portfolio and need innovative minds to help steer us into the future. In this case we are specifically looking for someone with a solid sourcing and category management toolkit as well as GxP experience in procurement. 

Summary:  The Process Engineer II, under the supervision of the Director of Engineering, will be responsible for performing engineering activities, new equipment/systems installation, new products introduction support, infrastructure assessments, troubleshooting support and technical expertise for process equipment and site utilities on behalf of the different facilities at Fujifilm Diosynth Biotechnology Texas (FDBT). Equipment support includes bioreactors, incubators, filtration skids, chromatography skids, centrifuge, autoclaves, freezers, refrigerators, walk-in cold rooms, QC/PD lab equipment, air cooled chillers, air compressors and dryers, air handling units, MCRs, MBUs, steam/water boilers, water purification and distillation units, wastewater treatment systems, among others.

This position will work closely with facilities, manufacturing resources, CAPEX team, validation, QA/QC and contractors to perform projects implementation and to help maintain complex process equipment and site utilities. This position will require involvement in the utilities and production processes to identify and implement process improvements using Change Control procedures as well as perform corrective and preventive actions using the CAPA system. This position will also support P&ID development, maintenance strategies development, SOP’s development and equipment commissioning/qualification activities as required. This position will also lead the identification of equipment of the proper type, size, materials, throughput, physical dimensions, required utilities and URS development for future projects.  

The Quality Control Analytical technologies (QCAT) group is seeking a dynamic Senior Scientist to manage the team-based execution of assay protocol driven activities for client programs.  The QCAT group is a technologically diverse group that primarily performs formal Tech Transfer, Qualification, Validation and Verification of test methods coming out of the development group and then transitions them into our Quality Control group. This high performing group is the interface between the development and quality groups and is responsible for ensuring long term success of the methods entering into QC.

The successful candidate will focus on creating analytical method protocols and summary reports (TT, qualification, validation and verification). The role will oversee individuals executing protocols, review data, ensure a seamless transition to the QC group in a manner that sets them up for “right first time” and prolonged execution success, troubleshoot issues/spearhead investigations, and work closely with the QA group and client SMEs throughout. The candidate will also be expected to follow cGMP documentation practices and initiate deviations, lab investigations, method revisions and other related activities within the quality system.

The Senior Engineer 1, EHS is responsible for leading the development and execution of Environmental, Health, Safety and Sustainability programs. This includes compliance with applicable regulations (Federal, State, Local), codes and standards. Serves as a subject matter expert (SME) and will collaborate with assigned functional operation areas to instill a world class culture of EHS. Additional responsibilities include support of EHS engagement programs (EHS observations, GEMBA), training, audits, inspections, investigations, and collaboration with EHS personnel across the organization.

We are hiring a Field Applications Scientist Intern. The Field Applications Scientist Intern will work with the Life Sciences Field Applications Team to lean existing processes and help drive project goals to completion.

We are hiring a Materials Management Supervisor. The Materials Management Supervisor will be responsible for leading the execution of materials management activities for warehousing optimization, inventory control accuracy, process improvements, and executing to department goals. They will be responsible for raw material and finished goods inventory levels and location control to support production schedules for three shifts.

As the Buyer, you will be responsible for managing all aspects of purchasing components from suppliers in order to assure timely delivery of parts to support production needs. In addition, the Buyer is the communication and logistical link between Planning, Operations, and the Supply Base. The Buyer is also accountable for managing supplier accounts with significant spend. In addition, the Buyer is expected to compile, interpret and analyze complex data in supporting commodity management team with supplier contracts.

This position is intended to serve as the primary point of contact between customers and service staff. In addition, participates in after-hours contact support, and provides administrative support to Service quality related functions.

As a Software Developer I, you will help the software team in the development of preclinical and clinical ultrasound imaging systems. In this role, you will work closely with senior software developers, contributing to all phases of the software development lifecycle. This position offers hands-on experience working with advanced ultrasound technology, providing opportunities to work on hardware control, graphical user interface design, data analysis and processing, and software infrastructure. Development work will primarily involve C++ and C# on the Microsoft Windows platform. As such, candidates should have a solid understanding of object-oriented programming in these languages, and work well in a fast-paced, collaborative environment.