Material Handler - All Shifts
Full-time
FUJIFILM Biotechnologies
Position Overview Join a high-impact team that keeps life-changing biopharmaceutical manufacturing running smoothly. As a Material Handler, you'll be the engine behind safe, compliant, and efficient material flow across GMP cleanroom environments-ensuring production teams have exactly what they need, when they need it. If you thrive in a fast-paced, highly regulated setting and take pride in precision, this is your moment. 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: Job Description What you'll do
- Cleanroom cleaning and disinfection
- Perform routine and periodic cleaning of manufacturing areas from Grade Controlled Non-Classified (CNC) through Grade C environments
- Clean and disinfect ceilings, walls, floors, surfaces, and equipment exteriors using approved agents
- Material handling and inventory control
- Execute material movements and transactions in SAP (or similar ERP): goods receipt, staging, transfer, consumption, and inventory adjustments
- Receive, inspect, and verify incoming materials against purchase orders and documentation
- Stage and deliver raw materials, consumables, and components to manufacturing in alignment with production schedules
- Maintain accurate inventory levels; support cycle counts and reconciliation activities
- Ensure proper labeling, status identification, and segregation of materials (released, quarantined, rejected)
- Complete required training and maintain compliance for Hazardous Waste Disposal
- Cleanroom and GMP operations
- Wipe down and transfer materials into CNC through Grade C areas following approved disinfection procedures
- Adhere to gowning requirements and aseptic practices when entering controlled environments
- Documentation and compliance
- Complete all required documentation in compliance with GMP and GDP standards
- Maintain accurate, real-time records of material movements and transactions
- Follow SOPs, batch records, and work instructions with exceptional attention to detail
- Equipment and area management
- Operate material handling equipment (e.g., pallet jacks, forklifts) safely and per site procedures
- Maintain cleanliness and organization of warehouse and staging areas using 5S principles
- Perform routine cleaning of workspaces and equipment as required
- Cross-functional support
- Collaborate with Manufacturing, Quality, and Supply Chain to ensure timely material availability
- Support production campaigns by ensuring continuous material flow to prevent downtime
- Assist with deviation investigations related to materials, as applicable
- Perform other duties, as assigned
- High school diploma or equivalent required with 1-3 years of experience in a GMP-regulated environment (biopharma, pharmaceutical, or medical device preferred); OR
- Associate's degree with 0-1 years of experience in a GMP-regulated environment (biopharma, pharmaceutical, or medical device preferred)
- Experience with SAP or similar ERP systems
- Associate's degree, preferably in Life Sciences or a related field
- 2+ years of direct experience in a cGMP manufacturing environment
- Proficiency in ERP or Warehouse Management Software
- Basic computer skills (SAP, Microsoft Office)
- Strong problem-solving, organizational, and time management skills
- Strong leadership and decision-making abilities
- Experience with advanced warehouse automation and optimization tools
- Ability to manage high-volume material operations
- Purposeful work: Help enable the production of critical therapies by ensuring flawless material flow
- Growth and learning: Expand your GMP, cleanroom, and ERP expertise in a collaborative environment
- Culture of excellence: Join a team that values safety, quality, accuracy, and continuous improvement
Vacancy posted 13 days ago
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