The Quality Control Chemist Lead, with limited supervision, will be responsible for mentoring the team on technical aspects of performing in-process, release and stability testing using the established analytical methods. This position is a pivotal role to either a technical career path as a Chemist IV or a managerial career path as a Lead for the team, and a successful individual in this role will lead the team regardless of the career path they decide to pursue.

Our Automation team in College Station, Texas is expanding and we are looking for Automation Engineers to provide technical and operational support, execution of critical projects, installation, operation, maintenance and troubleshooting of FUJIFILM Diosynth Biotechnologies Texas, LLC automation systems to meet organizational goals and objectives. This position will also work closely with other operators, technicians, managers and engineers to maintain complex systems.

The Strategic Finance Business Partner supports, challenges, and drives long-term strategic priorities, playing a pivotal role in formulating and understanding initiatives that drive long-term financial growth and profitability. This role closely collaborates with Senior Leadership to enhance business performance, conducts detailed analysis to deliver insights, and helps set strategic direction. By blending expertise in finance, strategic analysis, and planning, the Strategic Finance Business Partner guides the company’s Senior Leadership in achieving long-term goals.

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

The Microbiology IV will be responsible for the QC microbiological aspects of cGMP compliance and testing at the FUJIFILM Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory.  This position is a pivotal role to either a technical career path as a Microbiologist IV or a managerial career path as a Lead for the team, and a successful individual in this role will lead the team regardless of the career path they decide to pursue.

Reports to                Supervisor, Microbiology

Work Location         College Station, TX 

The Quality Control Raw Materials Chemist III, with limited supervision, will be responsible for participating in the Technology Transfer of established methods into the FUJIFILM Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory. Following Tech-Transfer Activities, the candidate will be responsible for performing in-process, release and stability testing using the established analytical methods.

Job Title: Quality Control Raw Materials Chemist III

Reports to: Quality Control Chemistry Manager

Summary: The Sr. Calibration Coordinator assists the Calibration team to ensure cGMP compliance and on time calibration work performed at Fujifilm Diosynth Biotechnology Texas (FDBT) facilities in College Station Texas. This individual will assist in implementing and scheduling the calibration of instruments and devices in the facility with an emphasis on planning and scheduling calibration. This individual may also assist in preparing SOPs and calibration instructions for the new systems entering the system, scheduling the periodic calibration of those instruments and the proper documentation when those instruments and devices may either fail calibration or be retired from the system.

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 hiring a R&D Project Manager I. The R&D Project Manager I will execute calculated risks and overcome challenges. They will plan, manage and coordinate R&D projects in a new product development Project to ensure that overall Project goals are met, lead large, complex product development efforts for multiple projects aimed at developing and manufacturing GMP-grade cell culture media, reagents and devices used for the production of biotherapeutics (e.g. monoclonal antibody therapies and vaccines), and regenerative medicine therapies (including stem cell therapy). They will be responsible for all new product development activities from concept through product launch, as well as tracking and reporting on post-launch activities.

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.

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. 

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.

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.