Senior Drug Product Manufacturing Associate

FUJIFILM Holdings America Corporation; Holly Springs (NC); On-site; USD 62,000 - 82,000; Full time

Benefits offered by this job

Competitive compensation

Comprehensive benefits package

Shift differentials

Mentor peers and training

Job summary

FUJIFILM Biotechnologies in Holly Springs, NC, seeks a Manufacturing Associate III to lead hands-on formulation, sterile filling, and visual inspection. The role supports dynamic DP facility startup, cGMP compliance, and cross-functional teamwork.

You will perform in-process tests, document quality steps, and help drive continuous improvement while adapting to a 24/7 shift with possible nights.

Qualifications

• High school diploma or GED with 4+ years direct experience in a cGMP manufacturing environment.
• Associate’s degree with 2 years direct experience in a cGMP manufacturing environment.
• Bachelor’s degree (pref Life Sciences or Engineering).
• Equivalent military training or experience.

Responsibilities

• Lead, execute, and document manufacturing processing steps and support activities.
• Perform in-process testing (pH, conductivity, visual inspection).
• Execute validation protocols per cGMP SOPs.
• Maintain training to perform all assigned activities.
• Assist and/or lead cycle counts; manage materials for the area.
• Operate DP unit operations: washing, autoclave, compounding, filling with isolator tech, visual inspection.
• Support improvement projects and training for new colleagues.

Skills

Teamwork

Communication

cGMP knowledge

Documentation

Safety awareness

Education

Bachelor’s degree in Life Sciences or Engineering

Associate’s degree (2 years)

High school diploma or GED + 4+ years cGMP

Equivalent military training

Tools

Parts washer

Autoclave operation

Isolator technology filling

Visual inspection equipment

Job description

FUJIFILM Biotechnologies in Holly Springs, NC, seeks a Manufacturing Associate III to lead hands-on formulation, sterile filling, and visual inspection. The role supports dynamic DP facility startup, cGMP compliance, and cross-functional teamwork.

You will perform in-process tests, document quality steps, and help drive continuous improvement while adapting to a 24/7 shift with possible nights.