Engineer I - 2º Shift

Amgen UK

Unknown, United Kingdom
Base: $88,281.00 - $119,439.00 usd annually; bonus...
8 years engineering/maintenance experience
Gmp biopharmaceutical production facility knowledge
Equipment troubleshooting and validation
This role involves joining the Facilities & Engineering group to partner with the corporate engineering team on designing, building, and qualifying new equipment for drug substance production

Job Summary

  • This role involves joining the Facilities & Engineering group to partner with the corporate engineering team on designing, building, and qualifying new equipment for drug substance production.
  • The successful candidate will provide system ownership for biopharmaceutical process equipment and lead technical root cause analysis to reduce production downtime.
  • Amgen offers a comprehensive benefits package including retirement plans, health coverage, and stock-based incentives while supporting a mission to serve patients living with serious illnesses.

Matching Summary

This role involves joining the Facilities & Engineering group to partner with the corporate engineering team on designing, building, and qualifying new equipment for drug substance production.

Salary

Base: $88,281.00 - $119,439.00 USD annually; Bonus/Equity: Discretionary annual bonus program and stock-based long-term incentives; Benefits: Comprehensive employee benefits package including retirement, medical, dental, vision, and flexible spending accounts

Skills & Requirements

Must-have

  • 8 years Engineering/Maintenance experience
  • GMP Biopharmaceutical Production facility knowledge
  • Equipment troubleshooting and validation
  • Root cause analysis implementation
  • 2nd shift work schedule availability

Nice-to-have

  • Bachelor's degree in Chemical or Mechanical engineering
  • Experience with cell culture reactors and chromatography
  • Strong leadership and technical writing skills
  • Ability to work in collaborative team-based environment
  • Understanding of capital project execution processes

Key Requirements

  • High school diploma/GED with 8 years experience OR Associate's with 6 years OR Bachelor's with 2 years
  • Direct knowledge of GMP Biopharmaceutical production equipment systems
  • Experience working in regulated environments (cGMP, OSHA, EPA)
  • Work schedule flexibility for 24/7 operations support

Work Rights

Not specified

Tailored Resume

Cover Letter