Sr Engineer I - Multiple Shifts

Amgen UK

Base: $115,494.60 - $156,257.40 usd; bonus/equity:...
10 years engineering experience or equivalent degree
Gmp biopharmaceutical production environment knowledge
Downstream unit operations expertise
This role involves partnering with the corporate engineering team to design, build, commission, and qualify new equipment for drug substance production

Job Summary

  • This role involves partnering with the corporate engineering team to design, build, commission, and qualify new equipment for drug substance production.
  • Candidates must ensure systems operate safely and remain compliant with GMP requirements while interacting with regulatory inspectors.
  • The position offers a competitive salary range of $115,494.60 to $156,257.40 USD along with comprehensive benefits including retirement plans and stock incentives.

Matching Summary

This role involves partnering with the corporate engineering team to design, build, commission, and qualify new equipment for drug substance production.

Salary

Base: $115,494.60 - $156,257.40 USD; Bonus/Equity: Discretionary annual bonus and stock-based long-term incentives; Benefits: Comprehensive health, dental, vision, retirement plan, and flexible spending accounts

Skills & Requirements

Must-have

  • 10 years engineering experience or equivalent degree
  • GMP Biopharmaceutical production environment knowledge
  • Downstream unit operations expertise
  • Root cause analysis and corrective action implementation
  • Equipment maintenance program development
  • System commissioning and validation in regulated environments

Nice-to-have

  • Data analytics and statistical process control skills
  • Six Sigma or predictive maintenance experience
  • Strong technical writing and presentation abilities
  • Collaborative team-based decision making style
  • Willingness to work rotational shifts and on-call support

Key Requirements

  • High school diploma with 10 years experience OR Bachelor's degree with 4 years experience
  • Bachelor's degree in Chemical or Mechanical Engineering preferred
  • 5+ years experience in Biopharmaceutical operations/manufacturing
  • Direct knowledge of chromatography, TFF, and CIP systems
  • Experience working in cGMP regulated environments

Work Rights

Not specified

Tailored Resume

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