Manufacturing Associate 3 - Upstream (Day Shift)
About The Position
This role will lead and execute manufacturing processing steps and associated activities. This role operates on a 2-2-3 schedule for Day Shift- 6A-6P. 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 What You’ll Do Lead, execute and document manufacturing processing steps and/or manufacturing support activities: Process monitoring and control Perform in-process testing (pH, conductivity, visual inspection) Execute validation protocols according to cGMP Standard Operating Procedures (SOPs) Maintain training to perform all required manufacturing activities Assist and/or lead cycle counts and manage materials for the assigned manufacturing functional area This role requires shift work (weekend and potential for nights) Perform other duties as assigned
Requirements
- High School Diploma or GED
- 4 years of related experience in a manufacturing environment
Nice To Haves
- BA/BS, preferably in Life Sciences or Engineering
- Associate’s Degree + 2 years of related experience in a cGMP manufacturing environment OR
- Equivalent Military training or experience
- Qualified experience on unit operation (DPFG Filler or Cell Culture – Seed Train)
- BioWorks or BTEC Capstone cGMP coursework preferred
Responsibilities
- Lead, execute and document manufacturing processing steps and/or manufacturing support activities: Process monitoring and control
- Perform in-process testing (pH, conductivity, visual inspection)
- Execute validation protocols according to cGMP Standard Operating Procedures (SOPs)
- Maintain training to perform all required manufacturing activities
- Assist and/or lead cycle counts and manage materials for the assigned manufacturing functional area
- Perform other duties as assigned
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
Number of Employees
501-1,000 employees
