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The successful Scientist II monitors ongoing experiments, identifies or resolves complex technical project issues, and provides technical leadership within the group. The individual takes a more active role in non-routine process development activities and may act as a technical lead for the analytical component of client programs.
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The Head of Program Management leads the Program Management function at the College Station, Texas site and is accountable for delivering customer programs from contract signature through program closure. This role combines ownership of program performance and customer experience with leadership of the site’s Program Management team.
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The successful Scientist I monitors ongoing experiments, identifies or resolves project issues, and provides technical leadership within the group. The individual takes a more active role in non-routine process development activities and may act as a technical lead for the analytical component of client programs.
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Lead a high-impact investigations team that safeguards product quality and patient trust. As Manager, Resilience (Drug Product Finished Goods), you’ll build and mentor a best-in-class investigations function, drive timely and high-quality resolutions to major and critical events, and be a visible leader during inspections—all while fostering a continuous improvement and people-first culture.
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The Weigh and Dispense Associate 1 is responsible for assisting with and executing the set-up, weighing of raw materials, solvents, and solutions. This role interacts with both Drug Substance and Drug Product teams as well as Warehouse for commercial operations and tech transfer activities required from the Weigh and Dispense operations. This role is responsible for weighing and dispensing in operations, plus duties to deliver goods to manufacturing, as needed. The Weigh and Dispense Associate 1 is required to work shiftwork, including nights and on-call.
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This position supports a 2/2/3 schedule from 6pm-6am.
The Senior Analyst 1, Quality Control (QC) All QC Team is responsible for performing routine testing required for Urgent/STAT testing of manufacturing batch samples, clean utility, environmental monitoring. This role is part of a 24x7 team that supports testing/sampling across all of the QC laboratories required for urgent testing/Manufacturing support. The role will learn and perform testing/sampling across multiple labs...
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This position supports a 2/2/3 schedule from 6pm-6am.
The Analyst, Quality Control (QC) All QC Team is responsible for performing routine testing requited for Urgent/STAT testing of manufacturing batch samples, clean utility, environmental monitoring. This role is part of a 24x7 team that supports testing/sampling across all of the QC laboratories required for urgent testing/Manufacturing support. The role will learn and perform testing/sampling across multiple labs in QC....
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The Senior Analyst 1, QC Microbiology is responsible for leading key operational aspects of the QC Microbiology laboratory. The Senior Analyst 1, QC Microbiology performs and trains other team members on the microbial testing of all in-process drug substance, drug product, EM/UM, and raw materials samples. This role is responsible for all activities associated with testing in accordance with written procedures. This role primarily works independently with minimal supervision as needed, consults with management on key decisions.
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The Engineering Documentation Specialist demonstrates complete and thorough understanding of Engineering turnover documentation and is responsible for day-to-day document management activities in a paperless environment. This role processes incoming and outgoing documents, including receipt, classification, registry, distribution, archive, storage, and retrieval. This role also serves as the administrator for project documentation management system and the subject matter expert (SME) for Good Manufacturing Practice (GMP) Engineering Management system.
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The Procurement Specialist 2, Business Partner, serves as an advisor and execution lead for sourcing, supplier management, and procurement optimization across assigned business units. This role partners closely with stakeholders to maintain P2P discipline and translate business needs into sourcing strategies that deliver value, mitigate risk, and ensure compliance. This role blends commercial acumen, stakeholder management, and procurement expertise with strong analytical and negotiation skills.
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Join a mission-driven team ensuring that every batch is safe, consistent, and inspection-ready. As an Engineer/Scientist 2 on our Process Validation team, you’ll help design, execute, and document robust validation strategies—partnering across Tech Transfer, Manufacturing, Quality, and Engineering to keep processes reproducible under normal operating conditions.
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Join a team where your upstream expertise directly impacts large-scale biologics production. If you enjoy solving complex challenges, leading technology transfers, and partnering with manufacturing to bring therapies to patients, this role offers the scope, autonomy, and collaboration to make a real difference.
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Help bring critical therapies to patients by executing and documenting cGMP manufacturing activities in a state-of-the-art, 24/7 facility. If you thrive in a team environment, are meticulous about documentation and safety, and enjoy hands-on work with meaningful purpose, this role is for you.
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The Supervisor, Maintenance is responsible for overseeing and coordinating the operations of maintenance systems and the team of process maintenance
technicians within assigned area to support Drug Product (DP) or Drug Substance Manufacturing (DSM) to ensure smooth and efficient operations. This
role focuses on maintaining and managing equipment, vendors, and daily operational activities while ensuring compliance with safety, regulatory, and
Good Manufacturing Practices (GMP) standards. Additionally, this role provides training, technical support, and leadership to the process maintenance
team.
Day Shift
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The Associate /Director, Maintenance role, leads the site maintenance organization, with end-to-end accountability for maintenance operations, maintenance
systems, reliability, spare parts, and MRO materials management. This role builds and sustains a Good Manufacturing Practice (GMP)
compliant, inspection-ready maintenance program that delivers safe, reliable, and available process, utility, and facility equipment in support
of large-scale biologics manufacturing. The Director shapes and executes the maintenance component of the site ramp-up strategy, scaling
the organization, processes, and systems as the site moves through qualification into routine...
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- This role is part of an invite-only hiring event.
- Candidates will be screened prior to scheduling.
- If selected, you’ll be asked to provide your availability for interviews on October 24.
- No walk-ins will be accepted on the day of the event.
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The Senior Analyst 1, QC Analytical Development (AD) Chemistry works with limited direction to support the execution of analytical method transfers and validations for drug substance (DS) and drug product (DP) manufacturing into the Quality Control laboratories of FUJIFILM Biotechnologies Holly Springs. The analytical chemistry methods used in biological product manufacturing include chromatography, spectroscopy, electrophoresis, wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc. The Senior Analyst 1, QC AD Chemistry adheres to GMP compliant laboratory operations in accordance with regulatory guidelines. This role executes analytical...
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The Analyst 1, QC Compendial Testing ensures laboratory operations are good manufacturing practices (GMP)-compliant according to United States\Europe\Japan pharmacopeia (USP/EP/JP) regulations. The role participates in the Technology Transfer (TT) of established methods into the FUJIFILM Biotechnologies, North Carolina Quality Control Laboratory. Following TT activities, the position performs material testing and disposition using the established analytical methods.
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We are seeking an Equipment Validation Engineer II to support the qualification of manufacturing equipment and utilities in our GMP facility. You will develop and execute risk-based validation strategies, author and run IQ/OQ/PQ protocols, and partner with cross-functional teams to ensure compliant, reliable operations.
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Senior QA Analysts for FUJIFILM Diosynth Biotechnologies Texas LLC, College Station, TX.
Responsible for review and/or approval of basic and technical documentation, drafting and reviewing internal Quality policies and procedures, performing product related activities, performing Quality audit functions, performing product release activities, identifying process and Quality System improvements, and acting as a QA liaison internally and externally for drug, biologics or vaccine products. Provide daily guidance, work prioritization and support to other...