Manufacturing Specialist , Drug Product Process

Help bring life-changing medicines to patients by ensuring reliable, compliant manufacturing. As a Manufacturing Specialist I, DP, you’ll be a hands-on problem solver and process SME who keeps operations running smoothly in a 24/7 environment-driving documentation excellence, tech transfer readiness, and continuous improvement across Drug Product Finished Goods.

FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we’ll open North America’s largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof. We’re looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we’re proud to cultivate a culture that will fuel your purpose, energy, and drive—what we call Genki.

Ready to shape the future of medicine? Let’s transform healthcare together! Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh’s thriving tech scene, making it the perfect blend of community and opportunity. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.”

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About Us We are a high-growth, 24/7 biopharmaceutical manufacturing site focused on delivering high-quality drug products safely and efficiently. Our team values collaboration, learning, and operational excellence. You’ll join a global, cross-functional community where your voice matters and your work makes a direct impact on patients.

• Support operational readiness during the project phase, including site commissioning and qualification efforts.
• Troubleshoot process issues and act as a process subject matter expert (SME) for assigned area(s).
• Coordinate batch planning, including process template creation, import, and the management of Preventative Maintenance (PMs).
• Own, perform, or drive major documentation updates (including initiating new documents for new processes).
• Coordinate non-batch activities such as changeover, PMs, and Aseptic Process Simulation (APS).
• Support MSAT with technology transfer activities within manufacturing.
• Ensure manufacturing operations adhere to all compliance and safety procedures.
• Create and update Electronic Batch Records (EBRs) and Paper Batch Records.
• Manage, perform, initiate, or support change management records, investigations, Corrective and Preventive Actions (CAPAs), and Continuous Improvement (CI) activities.
• Manage projects, lead execution, and participate in projects within Drug Product Finished Goods.
• Assist and support inspections and audits to ensure compliance in the manufacturing environment.
• Assist the Manager with projects and training, as needed.
• Collaborate effectively in small, cross-functional teams; mentor and guide junior associates.
• Flexibility with working hours and shift rotation to support a 24/7 manufacturing facility.

Within this role, you’ll be successful if you bring:

• Strong verbal and written communication skills.
• Strong time management skills.
• Ability to adapt in a fast-paced environment, pivot, and adjust plans accordingly.
• Ability to think critically and demonstrate superior problem-solving skills.
• Ability to analyze and troubleshoot simple to moderate system and component-related issues.
• Ability to coordinate and facilitate effective small cross-functional teams.
• Ability to mentor and guide junior-level associates.
• Ability to effectively present information to others.
• Team-based attitude…