DP Manufacturing Associate III - 24/7 Ops

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

Benefits offered by this job

Inclusive, team-first culture

Hands-on DP experience

Mentor peers and training

CGMP and technical training

Competitive compensation and benefits

Impact on patient medicines

Job summary

FUJIFILM Biotechnologies in Holly Springs, NC is seeking a Manufacturing Associate III to lead hands-on operations across formulation, sterile filling, and visual inspection in a state-of-the-art DP facility.

You will document processing steps, perform in-process testing, support qualification activities, and help coordinate shift tasks in a 24/7 environment, contributing to safe, compliant production that delivers high-quality medicines.

Qualifications

• Must have strong documentation and SOP adherence.
• Experience with at least one unit operation (e.g., autoclave, filling, inspection).
• Ability to operate in a regulated manufacturing environment.

Responsibilities

• Lead, execute, and document DP manufacturing steps with process monitoring.
• Perform in-process testing (pH, conductivity, visual inspection).
• Execute validation protocols per cGMP SOPs.
• Maintain training to perform all DP manufacturing activities.
• Assist in shift coordination and materials management for DP area.
• Support equipment qualification and DP facility startup.

Skills

Communication skills

Troubleshooting

Team collaboration

cGMP awareness

Safety procedures

Equipment knowledge

Education

Bachelor’s degree in Life Sciences or Engineering

Associate’s degree with 2 years experience

High school diploma or GED + 4+ years cGMP

Equivalent military training or experience

BioWorks or BTEC Capstone cGMP coursework

Job description

FUJIFILM Biotechnologies in Holly Springs, NC is seeking a Manufacturing Associate III to lead hands-on operations across formulation, sterile filling, and visual inspection in a state-of-the-art DP facility.

You will document processing steps, perform in-process testing, support qualification activities, and help coordinate shift tasks in a 24/7 environment, contributing to safe, compliant production that delivers high-quality medicines.