Sr Associate Quality Assurance

Amgen Inc

Base: $82,081.95 - $111,052.05 usd annually; bonus...
Onsite (shift-based)
Cgmp and gdp compliance knowledge
Shift work availability (afternoons/nights)
On-site presence required
Amgen is seeking a Sr Associate in Quality Assurance to support manufacturing operations and ensure compliance with Good Manufacturing Practices (GMP). The position involves on-the-floor quality oversight, real-time decision-making, and collaboration with manufacturing teams while working on a shift schedule

Job Summary

  • This role supports Amgen's mission to serve patients by ensuring adherence to cGMP quality requirements during bulk drug substance manufacturing.
  • The successful candidate will facilitate real-time decision-making and provide coaching on deviations, investigations, and compliance activities.
  • Amgen offers a comprehensive benefits package including retirement plans, health coverage, stock-based incentives, and flexible work models.

Matching Summary

Match Score: 85

Amgen is seeking a Sr Associate in Quality Assurance to support manufacturing operations and ensure compliance with Good Manufacturing Practices (GMP). The position involves on-the-floor quality oversight, real-time decision-making, and collaboration with manufacturing teams while working on a shift schedule.

Salary

Base: $82,081.95 - $111,052.05 USD annually; Bonus/Equity: Discretionary annual bonus and stock-based long-term incentives; Benefits: Comprehensive health, dental, vision, retirement plan, and flexible time-off

Skills & Requirements

Must-have

  • cGMP and GDP compliance knowledge
  • shift work availability (afternoons/nights)
  • on-site presence required
  • deviation investigation experience
  • CAPA and change control review

Nice-to-have

  • biotechnology plant startup experience
  • upstream/downstream manufacturing knowledge
  • EBR/MES and Delta V system proficiency
  • strong organizational and communication skills
  • team player with independent work ability

Key Requirements

  • High school/GED plus 4 years QA experience OR Associate's plus 2 years OR Bachelor's plus 6 months
  • Experience in regulated environment or pharmaceutical/biotech manufacturing
  • Willingness to transition to second or third shift schedule

Work Rights

Not specified

Tailored Resume

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