Filling Line Specialist – 2nd Shift, GMP

FUJIFILM Biotechnologies

Holly Springs (NC)

On-site

USD 60,000 - 90,000

Full time

3 days ago
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Job summary

FUJIFILM Biotechnologies in Holly Springs, NC, seeks a Manufacturing Associate to operate the filling line and support manufacturing projects. The role includes training teammates, scheduling daily activities, and ensuring GMP compliance.

The position involves shift work, with potential nights and weekends, and travel up to 25% during project phases. The facility aims to run 24/7, and the candidate will participate in validation activities and documentation packages, contributing to a robust

Qualifications

  • High School Diploma or GED required.
  • 4+ years in a cGMP manufacturing environment preferred with a Bachelor's degree.
  • Experience with drug product filling and related equipment is a plus.
  • Knowledge of GMP procedures, safety, and quality systems.
  • Ability to train coworkers and operate in a fast-paced, 24/7 facility.

Responsibilities

  • Lead, execute and document manufacturing steps and process monitoring.
  • Operate the Drug product filling line and related equipment.
  • Execute validation protocols per cGMP SOPs.
  • Develop processes and train coworkers to become trainers.
  • Maintain GMP documents and keep training current.
  • Support scheduling daily activities on the manufacturing floor.
  • Work with shift rotations; nights and weekends may be required.
  • Perform other duties as assigned.

Skills

Manufacturing experience
Shift work
Documentation
Training coworkers
cGMP knowledge
Quality systems
Process validation

Education

High School Diploma or GED
Associate's Degree + 4 years cGMP exp
BA/BS + 2 years cGMP exp
Equivalent Military training or experience

Tools

SOPs
Drug product filling equipment

Job description

FUJIFILM Biotechnologies in Holly Springs, NC, seeks a Manufacturing Associate to operate the filling line and support manufacturing projects. The role includes training teammates, scheduling daily activities, and ensuring GMP compliance.

The position involves shift work, with potential nights and weekends, and travel up to 25% during project phases. The facility aims to run 24/7, and the candidate will participate in validation activities and documentation packages, contributing to a robust

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