Sr. Associate Technical Engineer- Day Shift 12 Hour (6:00am-6:00pm)

Amgen Australia Pty Ltd

Base: $92,000.00 - $105,945.00 usd annually; bonus...
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Mechanical and electrical engineering support
Regulatory compliance with fda standards
Troubleshooting complex equipment failures
** Amgen Australia is seeking a Sr. Associate Technical Engineer for a day shift role focused on providing mechanical and electrical engineering support in the manufacturing of biotech products. The ideal candidate should have experience in technical engineering within a regulated environment, particularly in manufacturing and maintenance activities. **

Job Summary

  • This role provides critical technical mechanical and electrical engineering support to ensure equipment optimization and compliance with FDA standards.
  • The successful candidate will lead a team of technicians during breakdowns and assist in planning maintenance activities within a regulated pharmaceutical environment.
  • Amgen offers a comprehensive benefits package including retirement plans, health coverage, and opportunities for career development in a collaborative culture.

Matching Summary

Match Score: 75

** Amgen Australia is seeking a Sr. Associate Technical Engineer for a day shift role focused on providing mechanical and electrical engineering support in the manufacturing of biotech products. The ideal candidate should have experience in technical engineering within a regulated environment, particularly in manufacturing and maintenance activities. **

Salary

Base: $92,000.00 - $105,945.00 USD annually; Bonus: Discretionary annual bonus program; Benefits: Comprehensive health, dental, vision, retirement plan, and stock-based incentives

Skills & Requirements

Must-have

  • Mechanical and electrical engineering support
  • Regulatory compliance with FDA standards
  • Troubleshooting complex equipment failures
  • Experience with packaging equipment
  • Knowledge of GMP and cGMP regulations

Nice-to-have

  • Leadership experience leading technician teams
  • Familiarity with Maximo 7 software
  • Project management and continuous improvement skills
  • Training and technical guide development
  • Strong verbal and written communication

Key Requirements

  • Master's degree OR Bachelor's + 2 years experience
  • Associate's degree + 6 years experience
  • High school diploma + 8 years experience
  • Experience in regulated GMP/Pharmaceutical industry
  • Knowledge of PLC and serialization systems

Work Rights

Not specified

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