Manufacturing Associate 2 - Downstream (Day Shift)
About The Position
The Manufacturing Associate 2 executes and documents manufacturing processing activities per cGMP environment. This manufacturing facility will be 24/7 operational and the role may require to be flexible with working hours and shift rotation. 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
Requirements
- Knowledge of the operation of support process equipment
- Understanding of cGMPs, safety and operational procedures
- Ability to perform operations and document them accurately.
- Ability to follow technical instructions and document them.
- Ability to work closely and effectively in a team environment.
- Strong verbal and written communication skills
- Ability to adapt in a fast‐paced changing environment
- High School Diploma or GED and 2 years of related experience
Nice To Haves
- Associate degree, preferably in Life sciences or similar
- 2 years + direct experience in cGMP manufacturing environment
- Internal or after training: Qualified on a support area (i.e. Formulation Buffer Prep, Media Prep or DSM Buffer prep)
- BioWorks or BTEC Capstone cGMP coursework preferred.
Responsibilities
- During the project phase, Contributes to the preparation for operational readiness related to bulk drug substance manufacturing.
- Possible assignments include supporting projects related to, procedure review and/or creation, development or transfer of manufacturing business processes, testing and commissioning support
- Travel up to 0‐25% (international or domestic) may be required.
- In operations Executes and documents manufacturing processing steps and/or manufacturing support activities, process monitoring and control.
- Performs in‐process testing (pH, conductivity, visual inspection)
- Executes validation protocols according to cGMP Standard Operating Procedures (SOPs)
- Maintains training to perform all required activities.
- This role requires shift work (weekend and potential for nights).
- Performs other duties as assigned
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
