The Sr. Strategic Planner 1 role will be responsible for driving the Sales & Operations Planning at FLBN, Holly Springs site. This role will integrate commercial sales forecast with production planning, inventory strategy, and capacity for both Drug Substance and Drug Product/Finished Goods. This role will be a key liaison for strategic planning at the Holly Springs site between clients, production, and Site Leadership. This role will drive the Sales and Operational planning, balancing demands from our customers and production capacity. This role drives consistent communication and execution of the strategic planning, to include both short-term and long-term horizons, while working closely with internal stakeholders to optimize the production plan.

We are seeking a skilled and detail-oriented Senior Process Engineer dedicated to developing and optimizing transducer manufacturing processes. The ideal candidate will bring strong mechanical aptitude, hands-on experience with advanced subtractive manufacturing techniques, and a deep understanding of materials science—including metals, alloys, ceramics, composites, and adhesives. This role involves direct involvement in the preparation and processing of transducer acoustic stacks and arrays, as well as the development of new techniques to enable cutting-edge acoustic designs. As a key member of our team, you will play an essential role in improving product quality, increasing manufacturing efficiency, and expanding production capabilities through process troubleshooting and the adoption of innovative technologies.

Working collaboratively with cross-functional engineering, manufacturing, and operations teams, the Senior Process Engineer will drive continuous improvement using quality system tools and data-driven analysis, ensuring robust process documentation, traceability, and compliance with stringent manufacturing standards. The successful candidate will be self-motivated, an excellent communicator, and thrive in a dynamic environment that values technical expertise, problem-solving ability, and proactive innovation.

Territory Manager - Birmingham, AL - 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 market on the value of FUJIFILM Sonosite’s hand-carried compact ultrasound systems and tools. 

This position requires previous capital medical equipment sales experience.

To best serve the territory, prefer candidates currently located in the Birmingham, AL area

The Director, Drug Substance Manufacturing (DSM) plays a critical role in the design, execution, and leadership of DSM Operations strategy for the Holly Springs site. This role is accountable for all upstream and downstream manufacturing operations, ensuring safe, compliant, and successful delivery of life changing therapies for patients. The Director, DSM guides leaders, develops high-performing teams, and works cross-functionally to ensure alignment with our global network, including our partner site in Denmark. This role influences the long-term success of our site and partners with top-tier biopharmaceutical companies to manufacture cutting-edge medicines that change lives.

This position is intended to install, maintain, secure, and monitor HCUS’s network and server infrastructure including related software. Responsible for testing and implementation of new technology. Also responsible for developing IT policies and procedures and assisting the help desk with complex calls.

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 for QC testing.   

We have an exciting opportunity at our Mesa, Arizona facility for a QC Chemist!  The QC Chemist serves as a Quality Control Specialist responsible for analyzing semiconductor materials in support of product qualification and to support all Quality Control laboratory processes.

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 Process Engineer to support our CMP Slurry operations!

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 Process Engineers provide the technical support to design, develop, troubleshoot, and characterize high volume manufacturing processes in a safe, environmentally sound, and economic manner.

The Project Coordinator plays a crucial role in supporting HCUS initiatives by ensuring project parts and material groups are aligned and forecasted correctly.  This position requires strong coordination skills, attention to detail, and the ability to manage multiple tasks in a fast-paced environment. The ideal candidate will understand project management principles.  This position will report to the Manager of Project Management.  The next career level for a Project Coordinator will be Associate Project Manager if requirements are met.

The Associate Project Manager will play a pivotal role in supporting the execution of healthcare informatics projects, ensuring their timely delivery, high quality, and alignment with organizational goals.

This position requires a detail-oriented and organized individual capable of coordinating across teams, tracking project milestones, and ensuring compliance with HCUS standards. The successful candidate will collaborate with multiple stakeholders, including HCUS MI engineers, and other healthcare professionals, to deliver solutions that improve healthcare outcomes through innovative informatics.

The Reprocessing Engineer I is responsible for ensuring that Fujifilm Sonosite medical devices and accessories are designed to be cleaned and disinfected by customers in the field. This role operates within the Systems Engineering team and interfaces with specialists within the Hardware Verification, Mechanical Engineering, Product Management, and Clinical Engineering teams. This role will combine biology, chemistry, materials science, clinical workflows, and industry standards to develop well-established safe and effective disinfection procedures for medical ultrasound devices. The Reprocessing Engineer I will also provide guidance and leadership in the realm of sustainability, ensuring that FUJIFILM products are designed with materials and processes that have minimal impact on the environment.

The Sr. Analyst 1, QC Analytical Development (AD) Chemistry works with limited direction to support the execution of analytical method transfers and validations for drug substance (DS) and drug product (DP) manufacturing into the Quality Control laboratories of FUJIFILM Biotechnologies Diosynth Holly Springs (FDBN). The analytical chemistry methods used in biological product manufacturing include chromatography, spectroscopy, electrophoresis, wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc. The Sr. Analyst 1, QC AD Chemistry adheres to GMP compliant laboratory operations in accordance with regulatory guidelines. This role executes analytical method transfers from clients and authors and reviews procedures, SOPs, and technical reports.

The Sr. Analyst 1, QC Analytical Development (QCAD) Bioassay supports the implementation of plate and cell-based analytical methods for Technology Transfer (TT) of drug substance (DS) and drug product (DP) into the Quality Control laboratories of FUJIFILM Biotechnologies Diosynth Holly Springs (FDBN). This role supports the transfer and validation of methods such as residuals (HCP, DNA, Protein A), dot blot for product identity, ELISA ID/ Potency and various cell-based assays. The Sr. Analyst 1, QC AD Bioassay ensures Good Manufacturing Practices (GMP) compliant laboratory operations in accordance with regulatory guidelines. This role executes analytical method transfers from clients and author and review procedures, SOPs, and technical reports.

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.

The Supervisor, Weigh & Dispense is responsible for leading the Weigh & Dispense team and operations within Supply Chain to ensure compliant and reliable production. This position works closely with Raw Material Sampling to flex resources between Weigh & Dispense and Raw Material Sampling, optimizing staffing and productivity. The Weigh & Dispense team consists of multiple shifts in which this supervisor leads and oversees to support the demands of the production schedule, including night shifts, as needed.

The Senior Supply Chain Analyst role supports Supply Planning and Warehouse. Using both soft and technical skills, the analyst role works cross functionally with other areas (e.g., Manufacturing, Quality, and Process Science) to analyze data for future improvement and cost analysis. This role is both tactical and transformational by initiating, preparing and facilitating initiatives to build a strong Supply Chain for the future. The Senior Supply Chain Analyst contributes to establishing KPls and ensures transparent, unambiguous visual and verbal communication to drive optimization of stock levels for both cost and availability to support warehouse and production capacity.

The Quality Assurance (QA) Manager, QA Validation, will be responsible for the review and approval of commissioning/qualification/validation protocols, reports, and discrepancies.  The Manager will handle all associated responsibilities in compliance with FUJIFILM Biotechnologies quality policies and site SOPs to ensure regulatory compliance. 

Reports to                Director, QA Compliance

Work Location         College Station, TX 

The Production Scheduler, Drug Product Finished Goods is responsible for creating, maintaining, and optimizing daily and long-term production schedules across drug product manufacturing, filling, inspection, and packaging operations. This role ensures timely product delivery and efficient use of resources while adhering to current Good Manufacturing Practices (cGMP). Acting as a central coordination point, the scheduler partners with other departments (e.g., Manufacturing, Planning, Quality, Supply Chain) to align material availability, equipment capacity, and staffing needs with the production plan.