Manufacturing Associate 2 - Day Shift (2/2/3 6am-6pm)

Fujifilm • Holly Springs, NC

2d • Onsite

About The Position

We are hiring a Manufacturing Associate 2 to execute and document manufacturing processing activities in a cGMP environment. 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. 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 2 years of related experience (or equivalent combination of education and experience).
• 2+ years of direct experience in a cGMP manufacturing environment.
• Knowledge of support process equipment and understanding of cGMPs, safety, and operational procedures.
• Ability to follow technical instructions, perform operations, and document accurately.
• Strong verbal and written communication; ability to work effectively in a team.
• 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

• Associate degree, preferably in Life Sciences or a related field.
• Qualified in a support area (e.g., Formulation Buffer Prep, Media Prep, or DSM Buffer Prep) through internal or post‑hire training.
• BioWorks or BTEC Capstone cGMP coursework.

Responsibilities

• Contribute to project-phase operational readiness for bulk drug substance manufacturing.
• 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.
• 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.
• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED