24/7 Biomanufacturing Associate: Process & Compliance

FUJIFILM Holdings America Corporation; Holly Springs (NC); On-site; USD 65,000 - 90,000; Full time

Job summary

FUJIFILM Biotechnologies in Holly Springs, North Carolina, seeks a Manufacturing Associate 3 to assist with execution and documentation of manufacturing processing activities in a cGMP environment. The role supports project-phase readiness and steady-state operations in a 24/7 facility, with flexibility for shift rotations.

The position emphasizes teamwork, rigorous documentation, and adherence to procedures while contributing to safe, reliable production.

Qualifications

• High school diploma or GED with 4 years of related manufacturing experience; or
• Associate degree with 2 years of related manufacturing experience; or
• Bachelor’s degree with 0 years of related experience; or
• Equivalent military training or experience.

Responsibilities

• Contribute to operational-readiness activities for biopharmaceutical manufacturing.
• Support procedure creation, process transfer, equipment testing, commissioning, and validation activities.
• Independently execute and document manufacturing processing and support activities according to SOPs and cGMP requirements.
• Perform process monitoring and in-process testing, including pH, conductivity, and visual inspections.
• Operate assigned production equipment and perform qualified unit operations.
• Support basic troubleshooting and elevate operational concerns appropriately.
• Assist with cycle counts and materials management within the assigned functional area.
• Maintain all required training and qualifications.
• Support and guide less-experienced associates when appropriate.

Skills

Teamwork

Communication

Adaptability

Education

High school diploma or GED

Associate degree

Bachelor’s degree

Equivalent military training

Job description

FUJIFILM Biotechnologies in Holly Springs, North Carolina, seeks a Manufacturing Associate 3 to assist with execution and documentation of manufacturing processing activities in a cGMP environment. The role supports project-phase readiness and steady-state operations in a 24/7 facility, with flexibility for shift rotations.

The position emphasizes teamwork, rigorous documentation, and adherence to procedures while contributing to safe, reliable production.