Formulation Technician Ii (8hr Days, Mon-fri)

PPD (Thermo Fisher) UK

Greenville, United States
On-site
Cgmp adherence
Aseptic filling area
Operate filling isolator
PPD (Thermo Fisher) is seeking a Formulation Technician II for their Greenville, North Carolina facility, responsible for producing sterile injectables in a cleanroom environment. The role requires adherence to GMP standards and involves various production and documentation tasks, along with physical demands such as lifting and standing for long periods

Job Summary

  • As a Formulation Technician II, you will play a vital role in producing sterile injectables and working on moderate-scale problems that require analysis and critical thinking.
  • Complete tasks vital to manufacturing drug products in an aseptic filling area, including cleaning cGMP areas, performing line changeovers, parts preparation, filter integrity testing, operating parts washers and autoclaves, performing tray loading and unloading, operating the filling isolator, and general material handling.
  • We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges.

Matching Summary

Match Score: 75

PPD (Thermo Fisher) is seeking a Formulation Technician II for their Greenville, North Carolina facility, responsible for producing sterile injectables in a cleanroom environment. The role requires adherence to GMP standards and involves various production and documentation tasks, along with physical demands such as lifting and standing for long periods.

Skills & Requirements

Must-have

  • cGMP adherence
  • aseptic filling area
  • operate filling isolator
  • hazardous/toxic materials handling
  • cleanroom gowning procedures

Nice-to-have

  • troubleshoot equipment alarms
  • work with hazardous materials
  • team environment collaboration

Key Requirements

  • High school diploma or equivalent
  • Minimum of 1 year manufacturing experience
  • Experience in a cGMP environment preferred

Work Rights

Not specified

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