3 6am-6pm)

Fujifilm•Holly Springs, NC

3d•Onsite

About The Position

We are hiring a Manufacturing Associate 4 to lead and execute manufacturing processing activities in a cGMP environment. In this senior role, you will support both project-phase readiness (procedures, process transfer, testing/commissioning) and steady-state operations in a 24/7 facility—helping ensure safe, consistent, and efficient production of drug substance. You will also assist with daily scheduling and materials oversight for the manufacturing team. 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.”

Requirements

High School Diploma or GED and 6+ years of experience in life sciences manufacturing; or Associate degree and 4+ years of experience in life sciences manufacturing; or BA/BS and 2+ years of experience in life sciences manufacturing; or Equivalent military training/experience.
Advanced understanding of manufacturing run cadence and order of shift activities.
Knowledge of cGMPs, safety, and operational procedures; strong troubleshooting ability.
Demonstrated expertise with operation of specific production equipment.
Ability to follow technical instructions, execute operations, and document accurately.
Strong verbal and written communication; effective team collaboration skills.
Strong time management; ability to adapt in a fast-paced, changing environment.
Willingness to work shifts (including weekends/nights) and travel up to 0–25% as needed.

Nice To Haves

BioWorks or BTEC Capstone cGMP coursework.

Responsibilities

Contribute to operational readiness for bulk drug substance manufacturing during the project phase.
Support procedure review/creation and development or transfer of manufacturing business processes.
Provide testing and commissioning support for equipment/systems; travel up to 0–25% (domestic or international) may be required during the project phase.
Lead, execute, and document manufacturing processing steps and support activities; perform process monitoring and control per cGMP standards.
Perform in-process testing (e.g., pH, conductivity, visual inspection).
Execute validation protocols according to cGMP Standard Operating Procedures (SOPs).
Maintain required training and qualifications for all assigned activities.
Assist and/or lead cycle counts and manage materials for the assigned manufacturing area.
Support and/or assist senior-level associates or the supervisor with scheduling daily activities on the manufacturing floor, as needed.
Work assigned shifts in a 24/7 operation, including weekends and potential nights.
Perform other duties as assigned.

Benefits

Equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.

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