Sr Engineer I - 2º Shift

Amgen Australia Pty Ltd

Base: $115,494.60 - $156,257.40 usd annually; bonu...
10 years engineering experience or equivalent degree
Gmp biopharmaceutical production facility knowledge
Root cause analysis and corrective action implementation
This role involves partnering with the corporate engineering team to design, build, and qualify new equipment for drug substance production

Job Summary

  • This role involves partnering with the corporate engineering team to design, build, and qualify new equipment for drug substance production.
  • Candidates must ensure systems operate safely in alignment with GMP requirements and interact with regulatory inspectors during audits.
  • The position offers a competitive benefits package including retirement plans, health coverage, and stock-based long-term incentives.

Matching Summary

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

Salary

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

Skills & Requirements

Must-have

  • 10 years engineering experience or equivalent degree
  • GMP Biopharmaceutical production facility knowledge
  • Root cause analysis and corrective action implementation
  • System commissioning and qualification expertise
  • 2nd shift availability (3pm to 11pm)

Nice-to-have

  • Six Sigma and Statistical Process Control skills
  • Predictive maintenance experience
  • Strong technical writing and presentation abilities
  • Collaborative team-based mindset
  • Willingness for domestic and international travel

Key Requirements

  • High school diploma plus 10 years experience OR Bachelor's degree plus 4 years experience
  • Bachelor's degree in Chemical or Mechanical Engineering preferred
  • 5+ years experience in Biopharmaceutical operations/manufacturing
  • Direct knowledge of downstream unit operations like chromatography and filtration
  • Experience working in regulated cGMP environments

Work Rights

Not specified

Tailored Resume

Cover Letter