Weigh & Dispense Operations Specialist

FUJIFILM Biotechnologies; Holly Springs (NC); On-site; USD 65,000 - 85,000; Full time

Job summary

FUJIFILM Biotechnologies in Holly Springs, NC seeks a Weigh & Dispense Specialist to drive compliant, reliable material handling and production support. The role requires meticulous attention to processes, adherence to safety, and collaboration across manufacturing teams to ensure timely delivery of materials and accurate documentation.

The position emphasizes ownership of SAP-based material release, batch planning, and continuous improvement within a regulated biopharma setting, contributing to

Qualifications

• Experience in cgmp manufacturing operations
• Knowledge of SAP/materials management is a plus
• Strong documentation and record-keeping practices
• Ability to work in a regulated environment

Responsibilities

• Release process orders for operations and coordinate material deliveries in SAP
• Coordinate material deliveries with warehouse to support production schedule
• Troubleshoot discrepancies and act as SME for their process area
• Create/update documents (WI, SOPs) for new processes
• Support shift planning and staff training on equipment and systems
• Ensure compliance with safety procedures and CAPAs/CI activities
• Assist with large-scale improvement projects in DSM/DPFG
• Provide shop floor support and daily work plans

Skills

operations sequencing

change management

communication

time management

adaptability

teamwork

Education

High School Diploma or Equivalent

Bachelor's degree

Master's degree

Tools

SAP ERP

Job description

FUJIFILM Biotechnologies in Holly Springs, NC seeks a Weigh & Dispense Specialist to drive compliant, reliable material handling and production support. The role requires meticulous attention to processes, adherence to safety, and collaboration across manufacturing teams to ensure timely delivery of materials and accurate documentation.

The position emphasizes ownership of SAP-based material release, batch planning, and continuous improvement within a regulated biopharma setting, contributing to