Biopharma Manufacturing Associate III — 24/7 Operations

FUJIFILM; Holly Springs (NC); On-site; USD 25,000 - 33,000; Full time

Job summary

FUJIFILM Biotechnologies in Holly Springs, NC, is hiring a Manufacturing Associate 3 to execute and document biopharmaceutical processing in a cGMP environment. The role supports readiness and steady-state operations in a 24/7 facility and requires flexibility with shifts.

Responsibilities include procedure creation support, equipment testing, validation activities, and documentation per SOPs. You will work in a team to ensure safe, compliant production and assist with training less-experienced

Qualifications

• Must have 4+ years manufacturing experience with HS diploma or GED.
• Associate degree + 2+ years manufacturing experience.
• Bachelor’s degree + 0 years 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 (pH, conductivity, visual inspections).
• Operate assigned production equipment and perform qualified unit operations.
• Support basic troubleshooting and elevate operational concerns as needed.
• Assist with cycle counts and materials management within the area.
• Maintain all required training and qualifications.
• Support and guide less-experienced associates when appropriate.
• Perform other duties as assigned.

Skills

cGMP knowledge

Equipment operation

Shift coordination

Troubleshooting

Teamwork & communication

Education

HS Diploma / GED + 4 yrs experience

Associate degree + 2 yrs experience

Bachelor’s degree + 0 yrs experience

Equivalent military training

Job description

FUJIFILM Biotechnologies in Holly Springs, NC, is hiring a Manufacturing Associate 3 to execute and document biopharmaceutical processing in a cGMP environment. The role supports readiness and steady-state operations in a 24/7 facility and requires flexibility with shifts.

Responsibilities include procedure creation support, equipment testing, validation activities, and documentation per SOPs. You will work in a team to ensure safe, compliant production and assist with training less-experienced