Engineer I

Amgen Inc

Thousand Oaks, California, United States
Base: $88,281.00 - $119,439.00 usd annually; bonus...
Onsite
Master's degree or equivalent experience
2+ years engineering experience
Cgmp procedures knowledge
Amgen Inc is seeking an Engineer I to support manufacturing processes at their Thousand Oaks, California facility. The role involves operational support, troubleshooting, and optimization of equipment in a regulated biotech environment, with a strong emphasis on collaboration and continuous improvement

Job Summary

  • Amgen is seeking an Engineer I to support manufacturing processes in the Thousand Oaks Pilot Plant while serving patients living with serious illnesses.
  • The role involves providing operational support, troubleshooting, and optimization for assigned equipment including stainless and single-use systems.
  • Candidates will benefit from a comprehensive employee benefits package including retirement plans, health coverage, and flexible work models where possible.

Matching Summary

Match Score: 85

Amgen Inc is seeking an Engineer I to support manufacturing processes at their Thousand Oaks, California facility. The role involves operational support, troubleshooting, and optimization of equipment in a regulated biotech environment, with a strong emphasis on collaboration and continuous improvement.

Salary

Base: $88,281.00 - $119,439.00 USD annually; Bonus/Equity: Discretionary annual bonus program and stock-based long-term incentives; Benefits: Comprehensive health, dental, vision, retirement plan, and flexible time-off

Skills & Requirements

Must-have

  • Master's degree or equivalent experience
  • 2+ years engineering experience
  • cGMP procedures knowledge
  • Equipment troubleshooting skills
  • Root cause analysis capability

Nice-to-have

  • Six Sigma or Statistical Process Control
  • Maximo asset management system
  • Chromatography and filtration systems
  • Continuous improvement mindset
  • Mentorship experience with peers

Key Requirements

  • Master's degree OR Bachelor's + 4 years exp
  • Direct experience with regulated environments (FDA/cGMP)
  • Hands-on experience with complex manufacturing equipment
  • Knowledge of Maximo or equivalent asset management
  • Experience with corrective and preventative actions

Work Rights

Not specified

Tailored Resume

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