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Help power reliable, compliant, 24/7 biomanufacturing. As a Manufacturing Support Associate 3, Training (Downstream Manufacturing), you’ll be a hands-on technical leader who drives operational readiness, leads troubleshooting, and champions training and documentation excellence—so teams can produce safely, consistently, and on time.
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The Laboratory Scientist/Engineer 2 is part of a manufacturing science lab that serves as the first point of entry for external client processes to execute process establishment runs within a tech transfer framework. This position plans and executes bench-scale bioreactor studies (up to ~5 L fed-batch) and performs downstream purification, including chromatography and ultrafiltration/diafiltration (UF/DF). The role also generates data packages that enable scale-up and tech transfer to clinical and commercial manufacturing. The Laboratory Scientist 2 supports bridging studies, satellite runs, and ad-hoc investigations for large-scale manufacturing in close collaboration with internal partners...
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The Clean Utilities Engineer 3 provides engineering support to field personnel in the performance of maintenance and operational tasks associated with Clean Utilities, including reverse osmosis/electrodeionization (RO/EDI) skids, water for injection (WFI), purified water (WPU), Clean gasses and applicable waste systems. This role works directly with other Utility Engineers ensuring applicable safety and regulatory standards are maintained, identifies process improvements, and assists with troubleshooting equipment issues to maintain overall plant reliability. Additional...
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Win the programs that shape the future of cell and gene therapies. As FUJIFILM Biotechnologies’ Business Development Director for Advanced Therapies, you’ll own growth across the FUJIFILM Life Sciences Cell Therapy network—including FUJIFILM Biotechnologies, FUJIFILM Biotechnologies California, FUJIFILM Biotechnologies Texas (Viral Gene Therapy) and FUJIFILM Cellular Dynamics—turning cutting-edge science into scalable, GMP-ready solutions.
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Win the programs that shape the future of cell and gene therapies. As FUJIFILM Biotechnologies’ Business Development Director for Advanced Therapies, you’ll own growth across the FUJIFILM Life Sciences Cell Therapy network—including FUJIFILM Biotechnologies, FUJIFILM Biotechnologies California, FUJIFILM Biotechnologies Texas (Viral Gene Therapy) and FUJIFILM Cellular Dynamics—turning cutting-edge science into scalable, GMP-ready solutions.
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The Senior Analyst 1, QC Compendial Testing ensures laboratory operations are Good Manufacturing Practices (GMP)-compliant according to United States/Europe/Japan (USP/EP/JP) regulations. The role participates in the Technology Transfer (TT) of established methods into the Quality Control Laboratory as well as performs material testing and disposition using the established analytical methods.
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The QA Engineer, Drug Substance Manufacturing (DSM) Operations is responsible to help drive the Quality oversight for the direction of all Drug Substance Manufacturing (DSM) processes through to operational readiness during project phase. This role is responsible for quality assurance oversight of day-to-day activities and resolution or mitigation of issues.
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The EHS Associate 2 role is a highly visible, trusted partner to Operations—present at the Gemba, quick to support, and committed to enabling safe, high-quality work. In this role, you will respond to day-to-day questions, assist with incident investigations, and risk assessments, support GEMBA walks and audits, and help teams integrate EHS into standard work. Your focus is to listen, coach, and collaborate so that every colleague can do their best work safely, every shift.
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Job Title:QA Supervisor – Regulatory Affairs
Worksite: Bryan, TX
Requisition # 2026-38809
Job Description: QA Supervisor – Regulatory Affairs for FUJIFILM Diosynth Biotechnologies Texas LLC, Bryan, TX. Responsible for supporting the...
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Help build reliable, compliant manufacturing from day one. As a Manufacturing Support Associate 3, Tech Transfer, you’ll be a hands-on process expert who leads operational readiness, drives troubleshooting, and keeps production running smoothly in a 24/7 facility—while upholding the highest standards of safety, quality, and documentation.
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The Facilities Engineering Compliance Coordinator supports the compliant operation of facilities, utilities, and critical systems by coordinating documentation and follow-up for deviations, CAPA, effectiveness checks, and change controls. The role maintains data integrity, training acknowledgments, and record accuracy within applicable systems (e.g., CMMS, document control, quality systems). In collaboration with Engineering, EHS, Quality, and Operations, the coordinator sustains a state of control, drives audit readiness, and helps improve compliance workflows to achieve on-time, right-first-time closures. This is an entry-level role (0–2 years) with training and mentorship provided.
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The Raw Material Sampler 2 position is responsible for sampling of materials and products. This role works with multiple functions to support operations (e.g., Warehouse, Supply Chain, Quality Control (QC)). The Raw Material Sampler 2 uses Systems and Applications Production (SAP) Enterprise Resource
Planning (ERP) system for inventory management and Laboratory Information Management System (LIMS) for sample management while operating in a good manufacturing practice (GMP) facility with standard operating procedures (SOPs).
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As an Upstream or Downstream Supervisor, you will lead and develop a team of manufacturing associates supporting the startup and ongoing operation of a large-scale biopharmaceutical facility. You will build team capability, execute training plans, support commissioning, qualification, and operational-readiness activities, and ensure work is performed safely, consistently, and in compliance with cGMP requirements. You will also coordinate cross-functional activities, manage shift priorities and escalations, maintain controlled documentation, support investigations and corrective actions, and drive continuous improvement. During operations, you and your...
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We are seeking a Facility Mechanic II. This role performs general to intermediate facility repairs/cosmetic improvements to plant facilities. Performs routine mechanical troubleshooting and preventive maintenance (PM) tasks.
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Set the quality bar for a site that manufactures tomorrow’s therapies. As Senior Director, QA, you will sit on both the Site Leadership Team (SLT) and the Global QA Leadership Team—shaping site quality aspirations, executing the global QA strategy, and hardwiring inspection readiness into daily operations. You’ll lead Quality Operations, Quality Systems, Quality Training, and Supplier Qualification, ensuring harmonized, compliant Quality Systems that keep our license to operate strong and our clients confident. If you’re an executive QA leader who builds high-performing teams and delivers excellence in a 24/7 GMP environment, this is your moment to make...
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Win the programs that shape tomorrow’s therapies. As FUJIFILM Biotechnologies' Business Development Director for Commercial Process Development (PD), you’ll own the full Business Development cycle—from identifying and qualifying opportunities to negotiating scope and closing signed contracts—focusing on early‑phase programs that scale from cell line development through pre‑clinical manufacturing to Phase 2. You’ll turn market insight into territory plans, build executive‑level relationships, and convert complex client needs into solutions that our teams can deliver—fueling growth for the organization and impact for patients worldwide.
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The Warehouse Associate 1 position is responsible for storage, handling, and distribution of materials and products. This role supports Warehouse operations in receiving, shipping, and/or logistics. The Warehouse Associate 1 works with multiple functions to support operations (e.g., Manufacturing, Quality, Process Sciences, and other customers). This role uses SAP ERP system for inventory management, cycle counting, and shipping activities while operating in a GMP facility with standard operating procedures (SOPs). This role requires shift work and/or weekend hours to support operations and is required to fulfill on-call responsibilities, as...
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Do you thrive in a fast-paced, highly regulated environment where precision, teamwork, and continuous improvement make a real difference for patients? Join our Drug Product team as a Manufacturing Associate III to lead hands-on operations across formulation, sterile filling, and visual inspection—while helping stand up and optimize a state-of-the-art DP facility.
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The Director, Quality Systems and Compliance provides strategic leadership for the site's Pharmaceutical Quality System (PQS), Audits and Inspections, Documentation Management, GxP Learning, and Quality Compliance programs. The role ensures sustainable inspection readiness, maintains compliance with global regulatory requirements, and drives continuous improvement across quality systems. The Director serves as a key site leader during customer audits and regulatory inspections and partners across functions to strengthen quality culture, data integrity, and operational excellence. The Director, Quality Systems and Compliance fosters a strong Quality Culture across teams and contributes to cohesive...
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The Program Quality Manager is responsible for programs from the point of Quality Agreement signature through program closure. This role ensures FUJIFILM Biotechnologies, Holly Springs provides services in alignment with our contracted commitment to clients and our company vision/mission (strategy and compliance). This role is the primary client liaison representing FUJIFILM Biotechnologies, Holly Springs Quality. The Program Quality Manager handles and/or supports an average load of 1-3 client programs.