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The QA Operations Specialist is responsible for providing quality oversight of the day-to-day manufacturing operations for Drug Substance Manufacturing. This is primarily achieved through record and data review, area inspection, and incident resolution.
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Help us deliver reliable, compliant biomanufacturing. We are hiring a Manufacturing Associate 4 to lead and execute manufacturing processing activities in a cGMP environment. In this senior role, you will support both project-phase readiness (procedures, process transfer, testing/commissioning) and steady-state operations in a 24/7 facility—helping ensure safe, consistent, and efficient production of drug substance. You will also assist with daily scheduling and materials oversight for the manufacturing team.
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Help us deliver reliable, compliant biomanufacturing. We are hiring a Manufacturing Associate 2 to execute and document manufacturing processing activities in a cGMP environment. You will support both project-phase readiness (procedures, process transfer, testing/commissioning) and steady-state operations in a 24/7 facility—helping ensure safe, consistent, and efficient production of drug substance
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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 Technician 2, Maintenance for Drug Product Finished Goods (DPFG) is responsible for the installation, maintenance, and repair of Drug Product (DP) related systems/equipment (e.g., filling line, automated inspection line, formulation, and isolation). This role ensures the systems meet the stringent requirements of pharmaceutical manufacturing, conducts regular inspections and preventive maintenance DP related equipment to ensure equipment is operating efficiently with minimal downtime.
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Thank you for attending the Women in Bio - RTP career fair on 25JUNE2026.
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Drive excellence in a fast-paced, 24/7 manufacturing environment. As a Manufacturing Support Associate III, you will lead critical readiness and operational activities that keep production compliant, reliable, and safe. You will serve as a process subject matter expert, coordinate complex planning, and champion improvements that elevate performance across the site. This facility operates around the clock; flexibility with working hours may be required.
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Launch your career at the intersection of problem solving, quality, and cross‑functional teamwork. As an Associate Investigator, you will support and perform minor investigations, learn systematic root‑cause techniques, and partner closely with manufacturing, quality, and operations to drive timely, compliant outcomes. You will help ensure investigations close on schedule and provide critical support to senior investigators.
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Ignite operational excellence in a 24/7 manufacturing environment. As a Manufacturing Specialist I, Training, you will strengthen compliant, reliable production by building capability on the floor, coordinating critical operations, and serving as a go-to subject matter expert. If you are passionate about hands-on manufacturing, teaching others, and driving continuous improvement, this role is for you.
This facility operates around the clock; flexibility with working hours and shift rotation is required. This...
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Help power a world‑class, 24/7 manufacturing operation by ensuring production runs safely, compliantly, and on schedule. As a Manufacturing Support Associate I with a documentation focus, you’ll be at the heart of operational readiness, record accuracy, and continuous improvement—enabling teams to deliver life‑changing products with confidence.
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The QC Associate I role in Quality Control Microbiology is crucial for performing operational functions of the QC Microbiology laboratory. This position holds the responsibility for conducting environmental and clean utility monitoring and standard microbiological assays. The incumbent will operate under guidance of laboratory supervisors and lead analysts, ensuring technical issues are promptly escalated to laboratory management. Tasks will be assigned to off-shift personnel where possible. Overtime and temporary shift changes will be required to support programs that have samples with short testing windows (e.g., bioburden 12-hours).
Shift: Sunday - Wednesday (7:00am - 5:00pm)
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Program Manager is accountable for the planning & delivery of programs from the point of contract signature (Scope of Work / Letter of Intent /
Contract) through program closure. The PM ensures we provide services in alignment with our contracted commitment to clients and our company
vision/mission (strategy and compliance). The PM typically handles an average load of 1-3 programs and receives coaching & guidance from the Head of
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The manufacturing associate in Drug Product Manufacturing will have a primary task for operation of filling line including all tasks related. This role will also support projects which influence manufacturing processes for DPM including training of others. This position will also support and assist in scheduling daily manufacturing activities for the team. This manufacturing facility will be 24/7 operational and the role may require to be flexible with working hours or shift rotation.
This position has a second shift schedule.
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The Technician 1, Maintenance for Drug Product Finished Goods (DPFG)- NIGHT SHIFT- is responsible for assisting with the installation, maintenance, and repair of Drug Product (DP) related systems and equipment (e.g., filling line, automated inspection line, formulation, and isolation). This role ensures the systems meet the stringent requirements of pharmaceutical manufacturing, conducts regular inspections and preventive maintenance to ensure the equipment is operating efficiently with minimal downtime.
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The Warehouse Associate 2 position is responsible for storage, handling, and distribution of materials and products. This role supports Warehouse operations in receiving, shipping, and/or logistics throughout FDBN and works with multiple functions to support operations (e.g., Manufacturing, Quality, Process Sciences), The Warehouse Associate 2 uses Systems Applications and Products (SAP) ERP system for inventory management, cycle counting, and
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Be the driving force behind world-class quality. As a Sr. Specialist I, QC Instrumentation, you will independently own the life cycle of QC analytical instruments—from qualification to decommissioning—ensuring they operate flawlessly, meet data integrity expectations, and stay in full compliance with regulatory requirements. If you’re passionate about elevating lab performance, partnering cross-functionally, and solving complex instrumentation challenges, this role is for you.
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The CQV Engineer 3 supports the commissioning and qualification of equipment and systems for the site. This role performs validation activities to include but not limited to equipment set up, building dashboards, creating work orders, managing protocols, and reading and reviewing documents. This role ensures equipment and systems comply with regulatory requirements and quality standards while ensuring a successful integration of CQV activities into site projects.
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The Sr CQV Engineer 1 leads the commissioning and qualification of equipment and systems of assigned area for the site. This role performs and leads the CQV team through the validation lifecycle, investigation of deviations and root cause analyses, and establishes standard operating procedures and other documents. This role collaborates with internal and external stakeholders to ensure strategies, equipment, and systems incorporate global standards and
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The Associate Director, Quality Control (Microbiology) is responsible for the effective management of the Quality Control Microbiology team to assure on time analysis of manufactured product and environmental monitoring samples. Responsible to assure all testing is performed in compliance with applicable regulations, company specifications, procedures, and policies at Fujifilm Diosynth Biotechnologies.
The Associate Director, Quality Control (Microbiology) is the site SME for Microbiology, with oversight of microbial and...
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Join a high-impact team where your curiosity, problem-solving, and drive to improve will make a tangible difference. As an Investigator I, you’ll execute minor internal manufacturing investigations, pinpoint root and contributing causes, and help shape effective corrective and preventive actions (CAPAs) that keep our operations running at their best. You’ll also partner with senior investigators on major investigations—gaining exposure, mentorship, and opportunities to grow.