We’re looking for people who share our passion, drive, and energy – what we call Genki – to join our team.”

Summary: The Scientist I, under general supervision, will help FDBT to develop new methods to support clients and adapt client-specific methods to FDBT instrumentation as well as helping to qualify and/or validate them.

Summary: The Technician I, under direct supervision, will assist in the preparation, transfer and development of analytical methods for in-process, and finished product including release testing and testing of critical reagents.

Summary: The Assistant Scientist is an entry level position within each of the Process Development groups. The individual will learn and assist in the development and characterization of customer programs, and technology transfer to the manufacturing and/or Quality control group…

Summary: The Associate Director, Program Management, with mentoring and support from the Head of Program Management and/or a Program Director, will be responsible for the planning and delivery of programs from the point of contract signature (Scope of Work/Letter of…

Summary: The Associate Director, Supply Chain – TBF 100 is responsible for delivering contracted product per the revenue forecast and as well as establishing the central production plan activities for the start-up of the new SATURN Project located at the…

Summary: The Associate Principal Scientist, Group Leader – Analytical Method Transfer will lead the AMT group and will directly oversee technical transfers, qualifications, and validations of analytical methods conducted at FDBT. Responsibilities will include ensuring the success of all protocol-driven…

Summary: The Associate Principal Scientist Group Leader is responsible for managing a group of scientists as the initial supervisor in the Science and Innovation organization. The individual will actively participate and lead projects in innovation research and scientific collaborations and…

The Associate Principle Scientist independently applies scientific and/or cross-functional knowledge to achieve project goals and provide technical and scientific leadership within the department. The individual will typically lead customer projects and as expected to complete technical assignments through the self-sufficient…

Summary: The Associate Scientist – Analytical Method Transfer (AMT) will function collaboratively and productively in a team devoted to ensuring the quality of effective analytical methods at FDBT. The individual should possess experience with several bioanalytical techniques that are used…

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…

Summary: The Calibration Coordinator assists the Calibration team to ensure cGMP compliance and on-time calibration work performed at Fujifilm Diosynth Biotechnology facilities in College Station Texas. This individual will assist in implementing and scheduling the calibration of instruments and devices…

Summary: The Calibration Technician I is responsible for maintaining and improving the cGMP Calibration Programs at the Fujifilm Diosynth Biotechnology Texas (FDBT) facilities in College Station Texas. This includes complex bio-pharma processing equipment such as Mobile Bio Processing Rooms, Mobile…

Summary: The Calibration Technician II is responsible for maintaining and improving the cGMP Calibration Programs at the Fujifilm Diosynth Biotechnology Texas (FDBT) facilities in College Station Texas. This includes complex bio-pharma processing equipment such as Mobile Bio Processing Rooms, Mobile…

Summary: The Calibration Technician III is responsible for maintaining and improving the cGMP Calibration Programs at the Fujifilm Diosynth Biotechnology Texas (FDBT) facilities in College Station Texas. This includes complex bio-pharma processing equipment such as Mobile Bio Processing Rooms, Mobile…

Summary: The CAPEX Project Coordinator, under the supervision of the Director of Engineering and Technology, will be responsible for the support of capital projects documentation through the management of initiation and close out documents, schedule tracking, and multi-departmental approval routing.

The Cell Biology Analyst I, under general direction, will be responsible for performing routine and non-routine quantitative and qualitative analysis of samples submitted to the Quality Control (QC) Laboratory.

Summary: The primary job responsibilities of this position will be scheduling the cleaning regiments for our three different locations, as well as reviewing the log books for all three sites.

Summary: The Director of Operations is responsible for the development & maintenance of systems and ways of working within process development. In addition the individual will be responsible for the development and subsequent management of a Technical Project Leadership function….

Summary: The Director, Program Management will be responsible for the planning and delivery of programs from the point of contract signature (Scope of Work/Letter of Intent/Contract) to project delivery including technology transfer, and taking a product/process from execution of a…

Summary: The Director, QA Compliance will be responsible for oversight of QA Compliance for cGMP manufacturing of monoclonal antibodies and Gene Therapy/Viral products. The individual will work with global and site Quality to implement, maintain and improve Quality Management Systems…

Summary: This is an experienced role with in-depth and specialized knowledge of cGMP documentation. This position can largely function with minimal or no supervisory oversight for routine duties such as document routing, tracking document review and approval process, maintaining Document…

Summary: The Document Control Specialist I, under general direction, will be responsible for routing and archiving company controlled documents. Documents include but are not limited to; Standard Operating Procedures (SOPs), production records (PRs), training records, validation documents, and policies.

Summary: The Downstream Manufacturing Technician I will work directly with viral purification (either whole particle or split particle), continuous flow centrifuge operation, and sucrose gradient separation, techniques for filtration and chromatographic separation (i.e. column chromatography and HPLC) and viral inactivation.

Summary: The Downstream Manufacturing Technician II will work directly with a range of purification technologies and equipment including centrifugation, sucrose gradient separation, filtration, chromatographic separation (i.e. column chromatography) and viral inactivation following aseptic technique and GMP procedures.

Summary: The Downstream Manufacturing Technician III will work directly with a range of purification technologies including continuous flow centrifugation, sucrose gradient separation, filtration technologies (TFF and depth), chromatographic separations (GE AKTA systems), and viral inactivation following aseptic technique in a…

Summary: The Downstream Manufacturing Technician IV will work directly with a range of purification technologies including: filtration technologies (TFF and depth), chromatographic separations (Single Use GE AKTA systems), viral inactivation, etc. following aseptic techniques and procedures in a cGMP environment.

Summary: The Drug Product Operations Technician I will work directly with the Vanrx SA25 Vial Filling Isolator, following aseptic techniques and procedures in a cGMP environment.

The Drug Product Operations Technician II will work directly with the Vanrx SA25 Vial Filling Isolator, following aseptic techniques and procedures in a cGMP environment.

The Drug Product Operations Technician I will work directly with the Vanrx SA25 Vial Filling Isolator,. following aseptic techniques and procedures in a cGMP environment.

Summary: The Drug Product Operations Technician IV will work directly with the Vanrx SA25 Vial Filling Isolator,. following aseptic techniques and procedures in a cGMP environment.

The Drug Product Operations Coordinator assists the Drug Product Manufacturing team to ensure Right-First-Time execution on the GMP manufacturing floor by developing and driving systems for readiness, compliance, and performance of new knowledge. The Drug Product Operations Coordinator will assist…

The Drug Product Process Engineer is a mid-level position in the Drug Product Operations department in support of the production of drug product in the Texas BioManufacturing Facility – 100 (TBF-100) and the Flexible BioManufacturing Facility – 200 (FBF-200) in…

Summary: The EHS Specialist, under the supervision of the Senior EHS Manager, will be responsible for development and application of various safety and compliance programs at Fujifilm Diosynth Biotechnologies Texas (FDBT). Programs include occupational health and safety, fire safety, emergency…

Summary The Temporary Environmental Monitoring Technician, under general direction, will be assisting with routine and non-routine environmental monitoring and other duties within the Quality Control (QC) Laboratory. This position has the primary responsibility of assisting with environmental monitoring. Other responsibilities…

Summary: The electronic Quality Management System (eQMS) Systems Administrator will be the Quality organization’s Subject Matter Expert (SME) as it relates to the configuration, implementation, analysis as well as the maintenance of the (eQMS) across multiple FDB facilities.

Summary: The Equipment Engineer III, under the supervision of the Associate Director, Facility Engineering, will be responsible for life cycle development of new process and utility equipment for both critical upstream and downstream processes, as well as clean utility equipment…

Summary: The Facilities Engineer I, under the supervision of the Associate Director, Facility Engineering, will be responsible for performing various aspects of engineering, operational and troubleshooting support for facilities, utilities and process equipment including but not limited to bioreactors, fermenters,…

Summary: The Facilites Engineer II, under the supervision of the Associate Director, Facility Engineering, will be responsible for performing various aspects of engineering, operational and troubleshooting support for facilities, utilities and process equipment including but not limited to bioreactors, fermenters,…

Summary: The Head of Operational Excellence is responsible for leading, managing, and delivering the site portfolio of process improvement projects at Fujifilm Diosynth Biotechnologies, Texas in order to achieve the annual company delivery and revenue plan and longer term strategic…

The Head of Program Management will be responsible for leading, directing and managing a team of Program Managers responsible for program delivery at Fujifilm Diosynth Biotechnologies in order to achieve the annual company revenue plan while providing outstanding customer service…

Summary: Lead and manage site sales and operations planning process to ensure alignment of functions and senior management to delivery of business goals for medium to long term.

Summary: The Technical Support I position is responsible for the setup and maintenance of FDBT’s desktop systems, client applications, maintenance of printers and documentation of assets. The incumbent will assist with System Operations, Programming, Networking, Telecommunications, System backups and Security.

Summary: The Maintenance Planner/Scheduler under the supervision of the Manager, Maintenance Operations is responsible for the planning, scheduling and performance of the maintenance program including the oversight of the Computerized Calibration & Maintenance Management System (CCMS/CMMS) in support of multiple…

Summary: The Maintenance Technician I, under the supervision of the Facilities Maintenance Supervisor, or designated supervisor will be responsible for performing various aspects of utilities, facilities and process equipment maintenance and support for the Texas Biological Facility (TBF), the Flexible…

Summary: The Accounting Manager is responsible for fiscal functions of the Company in accordance with generally accepted accounting principles and in accordance with financial management techniques and practices appropriate within the contract manufacturing industry. The Accounting Manager will be responsible…

Summary: The Manufacturing Associate Process Engineer – TBF 100 is a position in the Manufacturing Technology Support (MT&S) department in support of the SATURN Project located at the Texas BioManufacturing Facility – 100 (TBF – 100) in College Station, Texas….

Summary: The Manufacturing Compliance Coordinator leads the tracking, coordination, and closure of Manufacturing CAPAs, change controls and deviations, and assists in supporting the timely release and disposition of batches and other post-execution activities.

Summary: The Manager of Technical Operations is an integral management position overseeing the Technical Operations department supporting Gene Therapy Manufacturing. The Technical Operation Group, consisting of Manufacturing Readiness and Compliance Coordinators and Technical Operations Engineers, will provide Manufacturing technology, materials,…

Summary: The Manufacturing Readiness Coordinator assists the Manufacturing team to ensure right-first-time execution on the GMP manufacturing floor and on time starts by coordinating and delivering readiness milestones.

The Manufacturing Process Engineer I – TBF 100 is an entry-level position in the Manufacturing Technology Support (MT&S) department in support of the SATURN Project located at the Texas BioManufacturing Facility – 100 (TBF – 100) in College Station, Texas….

Summary: The Manufacturing Process Engineer – TBF 100 is a mid-level position in the Manufacturing Technology Support (MT&S) department in support of the SATURN mAb manufacturing facility located at the Texas BioManufacturing Facility – 100 (TBF – 100) in College…

Summary The Manufacturing Supervisor – Upstream will work directly with cell-culture and viral propagation techniques; cell-culture and bioreactor operations; bacterial and fermentation operations; pDNA, protein, and yeast-related operations; and aseptic techniques while following cGMP procedures. This individual will also supervise…

Summary: The Manufacturing Supervisor – Drug Product Operations will work directly with the processes associated with the Vanrx SA25 Automated Filling machine. This includes but is not limited to formulation, aseptic filling, vial inspection and vial labeling following cGMP procedures….

Summary: The Manufacturing Supervisor – Downstream will work directly with a range of purification technologies including continuous flow centrifugation, sucrose gradient separation, various filtration technologies (TFF & depth), chromatographic separations technologies (GE AKTA systems), and viral inactivation following aseptic technique…

Summary: As Marketing Specialist for FujiFilm Diosynth Biotechnologies Texas, LLC (FDBT) you will have responsibilities for the general day-to-day marketing activities required to support the Global Marketing Team and the FDBT Human Resources Team. This position will report directly to…

Summary: The Materials Management Specialist is responsible for drafting and implementing supply chain management procedures governing the receiving, warehousing, ordering, shipping and internal distribution of cGMP (current Good Manufacturing Practices) and non-GMP materials.

Summary: The Materials Management Specialist is responsible for drafting and implementing supply chain management procedures governing the receiving, warehousing, ordering, shipping and internal distribution of cGMP (current Good Manufacturing Practices) and non-GMP materials.

Summary: The Microbiology Analyst I will be responsible for assisting the QC microbiological aspects of cGMP compliance and testing at the FujiFilm Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory.

Summary: The Microbiology Analyst II will be responsible for the QC microbiological aspects of cGMP compliance and testing at the FujiFilm Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory.

Summary: The Microbiology Analyst III will be responsible for the QC microbiological aspects of cGMP compliance and testing at the FujiFilm Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory.

Summary: The Principal Biotechnology Process Scientist functions within a team environment to actively address complex issues within a Contract Development & Manufacturing Organization (CDMO). The individual is responsible for analyzing process technologies in support of new project proposals and will…

Summary: The Process Maintenance Lead Technician, under the supervision of the Process Maintenance Supervisor will be the individual primarily responsible for providing operational, maintenance, monitoring, and troubleshooting support for manufacturing process areas equipment in support of both the Texas Biological…

The Process Maintenance Technician, under the supervision of the Process Maintenance Supervisor will be the individual primarily responsible for providing operational, maintenance, and troubleshooting support for manufacturing process areas equipment in support of both the Texas Biological Facility (TBF) and…

Summary: The Engineer I functions within a team based organization to actively address complex cGMP manufacturing issues. The individual is responsible for analyzing process technologies in support of new project proposals and assist in the technical transfer into the manufacturing…

Summary: The Engineer II functions within a team based organization to actively address complex cGMP manufacturing issues. The individual is responsible for analyzing process technologies in support of new project proposals and assist in the technical transfer into the manufacturing…

Summary: The Biotechnology Process Sciences Technician I functions within a team based organization to actively address cGMP manufacturing requirements. The individual’s main responsibility is to obtain documentation for cGMP appropriate materials (raw materials and components), prepare item specifications for these…

Summary: The Process Sciences Assistant will work in direct contact with the Process Sciences and Project Management staff to facilitate the acquisition, and organization of process material certificates of compliance and related information.

Summary: The Program Director will be responsible for the planning and delivery of programs from the point of contract signature (Scope of Work/Letter of Intent/Contract) to project delivery including technology transfer, and taking a product/process from execution of a client…

Summary: Our Capital Project team in College Station, Texas is expanding and we are looking for a Project Engineer to ensure deliverables for his/her respective projects are well managed and in line with their stakeholders and company expectations. We are…

Summary: Our Capital Project team in College Station, Texas is expanding and we are looking for a Project Manager to ensure deliverables for his/her respective projects are well managed and in accordance with their stakeholders and company expectations. The Project…

JOB PURPOSE Working as part of the Fujifilm Diosynth (FDB) Enterprise Project Management Office (ePMO), the job holder will project manage and/or play a significant role in the delivery of projects which are part of the FDB Global Business Change…

Summary: This position will be responsible for knowing all the applicable Biomanufacturing regulations and ensuring that they are followed. This position will coordinate and document internal regulatory processes, such as internal audits, inspections, license renewals, or registrations. May compile and…

Summary: The Quality Assurance (QA) Manager of Operations, will be responsible for the overall performance of the QA Operations group. The Manager will handle all associated responsibilities in compliance with Fujifilm quality policies and site SOPs to ensure regulatory compliance.

Summary: The Quality Assurance (QA) Specialist, will be responsible for all aspects governing GxP training. The Specialist will handle all associated responsibilities in compliance with Fujifilm quality policies and site SOPs to ensure regulatory compliance.

Summary: 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 Diosynth Biotechnologies quality policies and site SOPs…

Summary: The Quality Assurance (QA) Specialist for Data Integrity will be responsible for the day to day running of the FDBT Data Integrity Program, performing data integrity assessments, gap confirmation and risk assessments, generate Remediation Plan, and categorize gaps based…

Summary: The Quality Assurance (QA) Specialist Supplier quality will be responsible for supporting the supplier quality program. The Specialist will assist with ensuring all suppliers of raw materials, consumables, and GMP services are qualified prior to use within the facility.

Summary The Cell Biology Analyst II will be responsible for participating in the Technology Transfer of established methods into the FujiFilm Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory.

Summary The Quality Control Cell Biology III will be responsible for assisting in the qualification of test methods for in-process and final products. Be able to work under minimal supervision. Perform advanced assays requiring precise analytical skills and understanding of…

Summary: The Quality Control 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…

Summary: The Quality Control Analyst position, under general direction, will be responsible for performing review of routine and non-routine quantitative and qualitative analysis of samples submitted to the Quality Control (QC) Laboratory. The data reviewer is responsible to ensure activities…

Summary: The Quality Control Cell Biology Lead, with limited supervision, will be responsible for overseeing day to day operations of the QC Cell Biology Group. This position will involve handing out daily assignments, ensuring assignments are completed within the given…

Summary The Quality Control Chemistry Manager, under general supervision, will be responsible for planning, organizing, directing, and evaluating routine activities of the QC staff as well as overseeing all raw material testing and release for use in GMP production. The…

Summary : The Quality Control Stability Coordinator will be responsible for carrying out supporting activities on the stability program according to current regulations. This includes working with Clients to draft stability protocols, physically setting up stability studies according to respective…

Summary: The Scientist I assists 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…

Summary: The Scientist I, under general supervision, will help FDBT perform innovation in support of Advanced Therapies by preparing AAV materials (full and empty particles), improve or develop analytical methods, evaluate cell lines and plasmid reagents, and collaborate with scientific…

Summary: The Scientist II independently designs, executes and interprets complex laboratory experiments and development activities with priorities set by supervisor/project lead to achieve project goals. The individual should display good technical knowledge and scientific understanding of downstream purification of viruses,…

Summary: The Scientist II independently designs, executes and interprets complex laboratory experiments and development activities with priorities set by supervisor to achieve project goals. The individual demonstrates a practical understanding analytical and/or virology, and applies knowledge in support of product…

The Senior Manufacturing Lead – Downstream will lead a team and work directly with a range of purification technologies including: filtration technologies (TFF and depth), chromatographic separations (Single Use GE AKTA systems), viral inactivation, etc. following aseptic techniques and procedures…

The Senior Manufacturing Lead – Upstream will lead a team and work directly with a range of technologies following aseptic techniques and procedures in a cGMP environment.

Summary: The Senior Quality Assurance (QA) Manager, Compliance will be responsible for the overall performance of the Quality Systems group. The Manager will handle all associated responsibilities in compliance with FUJIFILM Diosynth Biotechnologies quality policies and site SOPs to ensure…

Summary: The Senior Scientist – Analytical Method Transfer (AMT) will function collaboratively and productively in a team devoted to ensuring the quality of effective analytical methods at FDBT. The individual should possess broad scientific knowledge of bioanalytical techniques that are…

Summary: The Senior Scientist Upstream will provide technology leadership for the Upstream Process Development for a variety of technical platforms, provide technical support for associated regulatory filings, and improve processes or propose modifications to equipment to deliver improvements. The Senior…

Summary: The Sr. Validation Engineer, under general direction, will be responsible for drafting and executing Installation, Operational, and Performance qualification protocols for facilities, utilities, manufacturing equipment, quality control equipment, cleaning processes, and manufacturing processes across multiple GMP facilities as well…

Summary: The Site Services Supervisor, under the supervision of the Associate Director, Facilities Engineering, will be the individual primarily responsible for coordinating and managing the various contractors and staff that support the day-to-day operations of the FDBT facilities and grounds,…

Summary: The Sr. Principal Scientist Group Leader, Upstream Process Development, functions independently and productively in the Upstream Process Development Group actively engaged in process development within a team-based PD laboratory to support a wide variety of vaccine development projects. The…

Summary:  This position is responsible for the design, development, maintenance, and delivery of technical training for the Manufacturing organization.  Prepare training design documents and manage instructional design projects.  Create and own the train-the-trainer program. 

Summary: The Supply Chain Coordinator will develop and maintain integrated production planning and scheduling that encompasses materials to assure that supply targets are met. This position will be responsible for ordering and buying materials as well as tracking production and…

Summary The temporary Quality Control Chemist I, under general direction, will be responsible for performing routine and non-routine quantitative and qualitative analysis of samples submitted to the Quality Control (QC) Laboratory. The assignment will last up to, but not longer…

Summary: This position is responsible for assisting with the design, development, maintenance, and delivery of technical training. Assist in preparing training design documents and managing instructional design projects. Create and own specific train-the-trainer programs.

Summary: The Upstream Manufacturing Technician I will work directly with cell-culture and viral propagation techniques, buffer and equipment preparations, cell-culture and bioreactor operation, bacterial and fermentation operations, and aseptic technique following GMP procedures.

Summary: The Upstream Manufacturing Technician II will work directly with cell culture and viral propagation techniques, buffer and equipment preparations, cell culture and bioreactor operation, bacterial and fermentation operations, and aseptic technique following GMP procedures.

Summary: The Upstream Manufacturing Technician III will work directly with a range of technologies including cell-culture and viral propagation techniques; cell-culture and bioreactor operation; bacterial and fermentation operations; pDNA; Protein and Yeast related operations; as well as aseptic technique following…

Summary: The Manufacturing Technician IV will lead a team and work directly with a range of technologies following aseptic techniques and procedures in a cGMP environment.

The Utilities Maintenance Manager, under the supervision of the Director or Associate Director, Facilities Engineering, will be responsible to oversee all the plant and clean utilities equipment at the Texas Biomanufacturing Facility (B100), the Flexible Biomanufacturing Facility (B200) and the…

Summary: The Utilities Maintenance Technician I, under the supervision of the Facilities Maintenance Supervisor, or designated supervisor will be responsible for performing various aspects of utilities maintenance and support for facility including the Texas Biological Facility (TBF), the Flexible Biological…

Summary: The Utilities Maintenance Technician II, under the supervision of the Process Maintenance Supervisor will be primarily responsible for installing, maintaining and repair of electrical components and systems as well as providing operational, maintenance, and troubleshooting support for utilities equipment…

The Validation Engineer I, under general direction, will be responsible for drafting and executing validation protocols for facilities, utilities, manufacturing equipment and quality control equipment, as well as preparing validation final reports for the same.

Summary: The Validation Manager will be responsible for drafting and executing cleaning, process validation, utility, process systems and process support systems qualification test work. Preparing validation summary reports for the qualification and validation of systems used to manufacture drug or…

Summary: The Validation Specialist I, under direct supervision, will be responsible for drafting, executing protocols and preparing validation final reports for facilities, utilities, manufacturing and quality control equipment in a GMP environment.

Summary: The Validation Specialist II, under direct supervision, will be responsible for drafting and executing protocols and preparing validation final reports for facilities, utilities, manufacturing and quality control equipment in a GMP environment.

Summary: The Virology Technician II, under direct supervision, will assist in the culture and growth of cells and BSL-2 viruses for the support of V-AD and PD activities for multiple client projects. This individual will support assay development by performing…