The key focus of the role is to close sales and achieve assigned sales goals by building rapport and achieving customer satisfaction. This includes discovery of net new leads, recovery of lost accounts/opportunities, and cross and up-sell activities in small accounts.

Responsible for partnering with the Field Sales Manager (FSM) in their assigned territory or market segment and deliver qualified leads to the product specialist to assist in increasing total territory sales.

We are seeking a detail-oriented team player who has a strong desire to help others and who can excel in a fast-paced work environment. As a Service-Technical Support Representative, you will be responsible for answering incoming customer support calls and emails, troubleshooting ultrasound systems and accessories, processing Service orders, setting up shipments and returns of equipment, as well as other related customer service and technical support related tasks and needs.

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

We are hiring a Senior Counsel to provide strategic legal counsel for FUJIFILM Holdings America Corporation (HLUS) and its ink and chemicals manufacturing businesses. Reporting to the Division General Counsel, Electronics, M&A & Assistant Secretary, the Senior Counsel, will be responsible for handling all legal affairs relating to the ink and chemicals manufacturing businesses and the corporate and transactional matters for HLUS and its subsidiaries. These responsibilities include mergers, acquisitions, divestitures, corporate reorganizations, equity investment, corporate governance, and other general corporate matters.

The right candidate will be excited to join a growing company with a diverse portfolio of technology and manufacturing businesses. This attorney will work both independently and collaboratively and be a reliable legal resource and valued business partner for HLUS and its subsidiaries. Please include a cover letter and resume indicating your interest and expertise in this position. Applicants under serious consideration will be asked to submit a list of three supervisor references.

Our ideal candidate should reside in the Eastern US.

The Senior Manager, Quality Compliance is responsible for the day-to-day activities of the Pharmaceutical Quality Systems (PQS) team regarding Inspection Readiness, Site Internal Audits, and Quality Management Review (QMR). This role focuses primarily on creating and maintaining the site internal audit plan and performing associated audits. Additionally, the future-state of this role is to also lead and develop a Quality Assurance (QA) compliance team.

The Sample Management Analyst II, 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 II arranges sample shipments for outsource testing and shipments to Clients or other facilities and controls dispensing of samples for QC testing.   

As the Software Architect, you will help formulate the technical strategy for our ultrasound platforms working on a combination of short-term and long-term initiatives in order to increase our efficiency and effectiveness. You will also drive technology investments and architectural alignments. This role will also identify and drive cross-company initiatives with clearly defined outcomes and metrics. You will oversee the software architecture of all platforms, with ownership of software capability, re-use, quality and reliability. A key contributing decision maker about which technologies to use, how software should be architected, and the technical direction of our ultrasound platforms. This candidate has a passion for breaking down complex problems and identifying solutions that can be implemented by software teams. 

The Procurement Manager is responsible for executing procurement strategies and initiatives at the Morrisville site as directed by the Regional Procurement Lead. This role involves managing a dynamic team to ensure efficient day-to-day procurement operations while aligning with broader organizational objectives. The Procurement Manager focuses on maximizing value, optimizing processes, and ensuring compliance with procurement standards.

Summary:  

The Scientist I assist in the planning of, conducting, evaluating, and interpreting routine laboratory experiments. The individual monitors ongoing experiments and identifies and resolves or suggests alternates or solutions to complex occurrences. The individual understands and applies use of equipment, technology and materials associated with analytical development and related studies and projects. The individual takes a more active role in non-routine analytical or process development activities. 

This role is dedicated to driving operational excellence through the application of Lean methodologies within the Quality Control operations in a GMP environment. The successful candidate will have a passion for reducing waste, improving process efficiency, and enhancing overall quality.

Summary:  The Manufacturing Director – Gene Therapy is responsible for the planning, directing, and coordinating activities related to the manufacturing processes for the National Center for Therapudic Manufacturing (NCTM), and Flexible BioManufacturing Facility – 200 (FBF – 200), while maintaining a highly effective operation leading to the production of safe, efficacious and compliant therapeutics.  The Manufacturing Director/Sr. Director will work as the Value Stream Owner for the VGT Modality and all supporting departments to ensure appropriate Return on Sales. The Manufacturing Director will be responsible for the cGMP production, manufacturing and systems that support the manufacture of virus-related vaccines and biotherapeutic products in a BSL 2 state-of-art facility.

The Sales Specialist, Diagnostic Oncology, in the Invitro Diagnostics Division, is responsible for identifying, prioritizing, and establishing relationships with Key Accounts and Opinion Leaders within the Liver/Hepatology Medical Oncology community. Manage specific assigned geographic areas and successfully drive the FUJIFILM HCC Risk Biomarkers sales through that community. As assigned interface with Senior Management teams from major IVD manufacturers. Maintain a comprehensive understanding of IVD reagent systems, distribution modalities, as well as clinical performance and utility of assays.

The IP Counsel is a member of the FUJIFILM Holdings America Corporation (“HLUS”) Legal Department reporting to the Chief IP Counsel. The IP Counsel will work on intellectual property matters for HLUS and its subsidiary companies, both independently and in collaboration with members of the HLUS Legal Department and outside counsel.

Sr. Specialist 1, QC Lab Support works under moderate supervision, supporting and participating in QC activities related to investigations, deviations, OOS/OOT, CAPAs, and Change Controls. This role assists in creating and maintaining GMP documents and processes, collaborating with stakeholders and QA. This role contributes to customer contact and CLO communication to support QC capabilities in delivering materials and results. This role helps ensure QC compliance with policies and procedures. This role participates in project management and process improvement initiatives, developing skills in risk assessment. The role requires the ability to work effectively both independently and as part of a team, with growing cross-functional collaboration.

The Regional AD, Procurement is strategic role of developing world-class procurement processes and frameworks. This role is responsible for managing this function and work closely with Finance, Legal, other functions and 3rd parties to ensure procurement activities are carried out in accordance with company standards. This role will be building and leading a business-driven regional team while utilizing your previous experience and skills within procurement strategy, processes, and negotiation to ensure our procurement-related activities foster success of the organization.

We are hiring a Research Scientist – Formulation and Lyophilization. The Research Scientist – Formulation and Lyophilization will be responsible for leading formulation development studies to improve solubility, stability, and bioactivity of recombinant cytokines and growth factors, design and execute lyophilization cycles with a focus on reducing moisture content, improving cake appearance, and maintaining activity. They will evaluate excipients and delivery system compatibility for liquid and lyophilized formats (vials, bags, etc.), and provide scientific guidance to junior team members and support troubleshooting of formulation-related challenges.

This role will perform 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. 

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 Assurance (QA) Analyst II, under general direction, will be responsible for review and/or approval of basic and technical documentation; Drafting and reviewing of internal Quality policies and procedures; Assisting in and performing product related activities; Assisting in and performing Quality audit functions; Identifying process and Quality System improvements; Acting as a QA liaison internally.

Reports to                Supervisor/Manager, QA

Work Location         College Station, TX