Biopharma Manufacturing Associate 3: Upstream & Downstream

FUJIFILM Biotechnologies

Holly Springs (NC)

On-site

USD 38,000 - 48,000

Full time

3 days ago
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Job summary

FUJIFILM Biotechnologies in Holly Springs, NC is hiring a Manufacturing Associate 3 to support execution and documentation of manufacturing activities in a cGMP environment, including training, equipment operations, testing, and validation.

The role requires flexibility with shift rotations and will operate in a 24/7 facility, contributing to operational readiness and safe, continuous production.

Qualifications

  • High school diploma or GED with 4 years of related manufacturing experience.
  • Associate degree with 2 years of related manufacturing experience.
  • Bachelor's degree with 0 years of related experience.
  • 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.
  • Perform other duties as assigned.

Skills

Teamwork
Communication
Adaptability
Attention to detail

Education

High school diploma or GED
Associate degree
Bachelor's degree
Equivalent military training

Job description

FUJIFILM Biotechnologies in Holly Springs, NC is hiring a Manufacturing Associate 3 to support execution and documentation of manufacturing activities in a cGMP environment, including training, equipment operations, testing, and validation.

The role requires flexibility with shift rotations and will operate in a 24/7 facility, contributing to operational readiness and safe, continuous production.

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