Biopharma Manufacturing Associate 2 - Upstream/Downstream

NCBioImpact

Holly Springs (NC)

On-site

USD 42,000 - 65,000

Full time

37 hours ago
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Job summary

FUJIFILM Biotechnologies in Holly Springs, NC, is seeking Manufacturing Associate 1 and 2 to support biopharmaceutical manufacturing in a cGMP environment. The role emphasizes readiness, documentation, and compliance in a 24/7 facility.

Ideal candidates will have a HS diploma or GED, up to 2 years of experience, and be willing to work flexible shifts, including nights and weekends. Training and cross-functional collaboration are key parts of this role.

Qualifications

  • High school diploma or GED required.
  • 0–2 years experience; shifts in a 24/7 environment.
  • Basic knowledge of process equipment and cGMP safety.
  • Ability to document accurately using good documentation practices.
  • Willingness to work weekends/nights.
  • Strong verbal and written communication.
  • Team player and able to work in a fast-paced environment.

Responsibilities

  • Support operational-readiness activities for biopharmaceutical manufacturing.
  • Assist with procedure review, document preparation, testing, commissioning, and equipment-readiness activities.
  • Execute and document manufacturing processing according to SOPs and cGMP requirements.
  • Perform process monitoring and in-process testing (pH, conductivity, visual inspections).
  • Follow technical instructions and accurately document completed work.
  • Complete and maintain all required training and qualifications.
  • Work collaboratively with experienced associates, technical staff, and supervisors.
  • Follow all safety, quality, and operational procedures.
  • Perform other duties as assigned.

Skills

Verbal communication
Written communication
Teamwork
Adaptability
Safety awareness

Education

High school diploma or GED
Associate degree (preferred)

Job description

FUJIFILM Biotechnologies in Holly Springs, NC, is seeking Manufacturing Associate 1 and 2 to support biopharmaceutical manufacturing in a cGMP environment. The role emphasizes readiness, documentation, and compliance in a 24/7 facility.

Ideal candidates will have a HS diploma or GED, up to 2 years of experience, and be willing to work flexible shifts, including nights and weekends. Training and cross-functional collaboration are key parts of this role.

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