Manufacturing Associate 2, Visual Inspection (1st Shift)

Position Overview 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. Company Overview 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.” Visit: https://www.fujifilm.com/us/en/about/region/careers Job Description About Us We are a growth-focused biomanufacturing organization committed to operational excellence, patient safety, and a culture of continuous improvement. Our team members: Collaborate across functions to deliver high-quality drug product reliably and safely Embrace cGMP standards and robust training to maintain compliance Value inclusivity, respect, and diverse perspectives to drive better outcomes Invest in learning and professional development to build strong, sustainable careers Responsibilities During project/startup phases: Contribute to operational readiness for drug product manufacturing Support procedure review and/or creation; help develop or transfer manufacturing business processes Assist with testing and commissioning activities to bring equipment and processes online Travel up to 0–25% (domestic or international) as needed In routine operations: Execute and accurately document manufacturing processing steps and/or manufacturing support activities in a cGMP environment Monitor and control processes in accordance with Standard Operating Procedures (SOPs) Perform in-process testing (including pH, conductivity, and visual inspection) Execute validation protocols per cGMP SOPs Maintain all required training and qualifications for assigned activities Work a shift schedule after startup (includes weekends and potential nights) in a 24/7 operational facility Perform other duties as assigned to support team and business needs What you’ll bring to…