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 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…

We are ‘Advancing tomorrow’s medicines’ and making a real difference to the world in which we live. At Fujifilm Diosynth Biotechnologies, we partner with our clients to deliver recombinant proteins, viral vaccines and gene therapies to patients. As a Contract…

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…

The Downstream Process Development Associate Principal Scientist functions in a supervisory role in the Downstream Process Development Group, actively engaged and engaging others in process development within a team based PD laboratory. The individual will independently lead customer projects 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 – Upstream Process Development will assist in the development and execution of experiments for the development, optimization, and characterization of cell-based and viral vaccine processes and will be involved in experimental design, data analysis, and interpretation….

Summary: Our Automation team in College Station, Texas is expanding and we are looking for Automation Technicians to provide technical and operational support, execution of projects and improvements, installation, operation, maintenance and troubleshooting of FUJIFILM Diosynth Biotechnologies Texas, LLC automation…

The Biosafety Specialist II, under the supervision of the Senior EHS Manager/Biosafety Officer, will be responsible for the development and application of various safety and compliance programs at FUJIFILM Diosynth Biotechnologies Texas as they relate to the use of microorganisms,…

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…

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: To support the VP Commercial Development in development, maintenance and execution of strategies to strengthen the Gene Therapy (GT) commercial pipeline within Europe. This is a global position that will support all four sites (FDBU, FDBT, FDBK, and FDBD)….

Summary: The Commercial Development Specialist Lead will manage Commercial Development Specialist operations to ensure alignment of activities versus the goals of the wider Commercial Function, drive global harmonisation and prioritise workload against direction provided by the Commercial Leadership Team. This…

Summary: Support Executive Director, Global Alliance Manager and CBO in development, maintenance and execution of strategies to strengthen existing relationships and foster new relationships with Pharma and Key Accounts (P&K) to support the continued growth of FDB. Accounts with Strategic…

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…

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 Portfolio (GBCP)….

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,…

The Director, Facility Engineering will be responsible for the supervision of Fujifilm Diosynth Biotechnologies Facilities staff, consisting of twenty plus personnel of various skill sets, responsible for the building engineering, metrology activities, preventative and corrective maintenance of equipment, machinery and…

Summary: Provides organization and coordination of company revenue contract to delivery, provides customer proposal and contract review, and Program Profitability tracking.

The Head of Process Development provides strong scientific and administrative leadership to the Process Development and Process Sciences Departments, setting annual goals and objectives and long range planning. The Department Head creates high-level business strategy for the departments, oversees the…

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…

The Manufacturing Process Engineer I position is an integral part of the Manufacturing Technical Operations department, supporting Gene Therapy manufacturing at the National Center for Therapeutics Manufacturing (NCTM) and the Flexible BioManufacturing Facility (FBF200), located in College Station, Texas. This…

The Manufacturing Supervisor may be assigned to work directly with Upstream, Downstream or Buffer Preparation Unit Operations. This individual will supervise a team of employees directly or indirectly in these production process units.

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….

In order to be considered for this position, please apply here: https://www.spherion.com/job-seekers/jobs/q-manufacturing-technician/texas/bryan/ Summary: The Manufacturing Technician I and II work directly with a range of technologies. Dependent upon assignment, the range of technologies may include any of the following: Upstream…

Summary: The Manufacturing Technician III and IV will work directly with a range of technologies. The Technician IV level provides an opportunity to stay on the technical track, or work towards a supervisory path. Dependent upon assignment, the range of…

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: Under limited supervision of the Sr. Manager, Materials Management, the Materials Specialist II is responsible for the accurate receipt, verification, record keeping, distribution, and shipment of materials and goods.

Summary: Under limited supervision of the Sr. Manager, Materials Management, the Materials Specialist II is responsible for the accurate receipt, verification, record keeping, distribution, and shipment of materials and goods.

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 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: 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) Analyst III, under minimal direction, will be responsible for review and/or approval of basic and technical documentation, drafting and reviewing of internal Quality policies and procedures, performing product related activities, performing Quality audit functions, performing…

The QA – Supervisor – Compliance Specialist, will be responsible for the leading the compliance team with the management, metrics, and closure of CAPAs, Change Controls, Deviations, and Events. The Supervisor will handle all associated responsibilities in compliance with Fujifilm…

Summary: 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…

The Quality Assurance (QA) Specialist for Audit & Inspection will be responsible for supporting and client audits, regulatory inspections, conducting internal and supplier assurance audits.

The Quality Assurance (QA) Specialist – Compliance, will be responsible for supporting performance of the Quality Systems group. The Specialist will assist with the tracking and coordination and closure of Deviations, Events, Change Controls, and CAPAs.

The QA Validation Specialist will be responsible for the review and approval of commissioning/qualification/validation protocols, reports, and discrepancies for Quality Assurance. The QA Validation Specialist will handle all associated responsibilities in compliance with Fujifilm quality policies and site SOPs to…

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 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 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 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 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…

Summary: Collaborate with the VP Commercial Development to assist in developing and executing the commercial strategy in a specific territory or technology area with near term, mid-term and long term goals and objectives. This is a global position that will…

Summary: The Senior Scientist – Downstream Process Development, functions independently and productively in the Downstream Process Development Group actively engaged in process development within a team based PD laboratory. The individual should display strong technical knowledge and scientific understanding of…

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 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 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…

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 Project Manager will be responsible for managing the execution of multiple validation related projects at FDBT facilities.

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: Under limited supervision of the Sr. Manager/Manager, Materials Management, the Warehouse Specialist II is responsible for the accurate receipt, verification, record keeping, distribution, and shipment of materials and goods. Functional job responsibilities will include but are not limited to: