Director Non-sterile Operations

Thermo Fisher Scientific UK

Greenville, North Carolina, United States
Onsite (standard mon-fri)
Cgmp compliance in regulated environment
Leadership of non-sterile operations
Experience with auto injector assembly
Thermo Fisher Scientific is seeking a Director of Non-Sterile Operations in Greenville, NC, responsible for leading non-sterile manufacturing operations with a strong focus on packaging and assembly. The ideal candidate will have over 10 years of relevant experience in pharmaceutical manufacturing and a thorough understanding of cGMP regulations

Job Summary

  • The Director provides strategic and operational leadership for non-sterile manufacturing operations including packaging, inspection, and device assembly.
  • This role ensures safe, compliant, and efficient execution of activities from development through commercialization while driving operational excellence.
  • The position requires developing high-performing teams and fostering a culture of continuous improvement within the Drug Product Division.

Matching Summary

Match Score: 85

Thermo Fisher Scientific is seeking a Director of Non-Sterile Operations in Greenville, NC, responsible for leading non-sterile manufacturing operations with a strong focus on packaging and assembly. The ideal candidate will have over 10 years of relevant experience in pharmaceutical manufacturing and a thorough understanding of cGMP regulations.

Skills & Requirements

Must-have

  • cGMP compliance in regulated environment
  • leadership of non-sterile operations
  • experience with Auto Injector Assembly
  • oversight of Oral Solid Dose platforms
  • continuous manufacturing technology knowledge

Nice-to-have

  • strong financial and strategic acumen
  • ability to influence cross-functional stakeholders
  • culture of engagement and accountability
  • experience with automated assembly systems

Key Requirements

  • Bachelor's degree in Engineering or related field
  • 10+ years progressive operations leadership experience
  • Experience in cGMP-regulated pharmaceutical environment
  • Knowledge of FDA 21 CFR Parts 210/211 and 820

Work Rights

Not specified

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