Manufacturing Associate 3, Drug Substance — 24/7 Production

FUJIFILM Electronic Materials (Europe) N.V.

Holly Springs (MS)

On-site

USD 65,000 - 85,000

Full time

14 days+
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Benefits offered by this job

Competitive compensation with shift d
Comprehensive health and wellness plan
Retirement savings with company match
Paid time off and holidays
Training and career development

Job summary

FUJIFILM Biotechnologies is hiring a Manufacturing Associate 3 (Drug Substance Manufacturing) to lead core processing steps, support readiness for new capacity, and sustain a 24/7 operation.

You’ll perform in‑process testing, execute validation protocols, maintain training, and assist with cycle counts while collaborating across teams to ensure safe, compliant production and on‑time delivery.

Qualifications

  • Bachelor’s degree in Life Sciences or Engineering or equivalent.
  • 4 years of related manufacturing experience acceptable with HS diploma.
  • Strong understanding of cGMP, safety and SOPs.
  • Ability to troubleshoot and work in a 24/7 manufacturing environment.

Responsibilities

  • Lead, execute, and document manufacturing steps and monitoring.
  • Perform in-process testing (e.g., pH, conductivity, visuals).
  • Execute validation protocols per cGMP SOPs.
  • Maintain required training for assigned activities.
  • Assist with cycle counts and materials management; support 24/7 shifts.

Skills

Troubleshooting
Verbal and written communication
Production equipment operation
Manufacturing run cadence
cGMP knowledge
Team collaboration
Leadership potential

Education

Bachelor’s degree in Life Sciences or Engineering
Associate’s degree
High school diploma / GED + 4 years in manufacturing
Equivalent military training or experience

Job description

FUJIFILM Biotechnologies is hiring a Manufacturing Associate 3 (Drug Substance Manufacturing) to lead core processing steps, support readiness for new capacity, and sustain a 24/7 operation.

You’ll perform in‑process testing, execute validation protocols, maintain training, and assist with cycle counts while collaborating across teams to ensure safe, compliant production and on‑time delivery.

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