Engineer I - 2º Shift

Amgen Inc

Base: $88,281.00 - $119,439.00 usd; bonus/equity: ...
8 years engineering/maintenance experience
Gmp biopharmaceutical production facility knowledge
Equipment troubleshooting and root cause analysis
This role involves joining the Facilities & Engineering group to design, build, and qualify new equipment for drug substance production while supporting downstream process engineering

Job Summary

  • This role involves joining the Facilities & Engineering group to design, build, and qualify new equipment for drug substance production while supporting downstream process engineering.
  • The successful candidate will provide system ownership for biopharmaceutical process equipment, lead root cause analysis to reduce downtime, and ensure compliance with GMP requirements.
  • Amgen offers a competitive salary range of $88,281.00 - $119,439.00 USD along with comprehensive benefits including retirement plans, health coverage, and stock-based incentives.

Matching Summary

This role involves joining the Facilities & Engineering group to design, build, and qualify new equipment for drug substance production while supporting downstream process engineering.

Salary

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

Skills & Requirements

Must-have

  • 8 years Engineering/Maintenance experience
  • GMP Biopharmaceutical Production facility knowledge
  • Equipment troubleshooting and root cause analysis
  • Commissioning and qualification of systems
  • 2nd Shift availability (3pm to 11pm)

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 a 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 equipment such as autoclaves and CIP systems
  • Experience working in regulated environments (cGMP, OSHA, EPA)
  • Work schedule flexibility for 24/7 operations and rotational on-call support

Work Rights

Not specified

Tailored Resume

Cover Letter