Manufacturing Associate 4 - Downstream (Day Shift)

Fujifilm • Holly Springs, NC

3d

About The Position

This role as manufacturing Associate 4 will execute manufacturing processing steps and associated activities. This position will also support and assist in scheduling daily manufacturing activities for the team.
This role operates on a 2-2-3 schedule for Day Shift- 6A-6P.
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

• High school Diploma or GED and 6 years of experience in a life science’s manufacturing OR
• Associate degree + 4 years’ experience in a life sciences manufacturing OR
• BA/BS + 2 years’ experience in a life sciences manufacturing OR
• Equivalent Military training/experience

Nice To Haves

• Understanding of manufacturing run cadence and order of shift activities.
• Knowledge in cGMP, safety, and operational procedures
• A high degree of knowledge and expertise of the operation of specific production equipment
• BioWorks or BTEC Capstone cGMP coursework preferred

Responsibilities

• Leads, 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 manufacturing activities
• Assists and/or leads cycle counts and manages materials for the assigned manufacturing functional area
• Supports and/or assist senior level associates or supervisor with scheduling daily activities on manufacturing floor, as needed
• This role requires shift work (weekend and potential for nights)
• Performs other duties as assigned.

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