Sr Associate Quality Assurance

Amgen UK

Base: $82,081.95 - $111,052.05 usd annually; bonus...
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Cgmp and gdp compliance knowledge
Shift work availability including nights
On-site facility presence required
** Amgen UK is seeking a Sr Associate in Quality Assurance to oversee plant manufacturing and support quality compliance in a biotech environment. The position involves real-time decision-making to ensure adherence to Good Manufacturing Practices (GMP) and requires shift work, including late afternoons and nights. **

Job Summary

  • This role serves as a vital on-the-floor Plant Quality Assurance partner to ensure adherence to GMP quality requirements during bulk drug substance manufacturing.
  • The successful candidate will facilitate real-time decision-making, manage deviations, and drive the closure of corrective actions within a collaborative team environment.
  • Amgen offers a comprehensive benefits package including retirement plans, health coverage, and stock-based incentives to support professional growth.

Matching Summary

Match Score: 75

** Amgen UK is seeking a Sr Associate in Quality Assurance to oversee plant manufacturing and support quality compliance in a biotech environment. The position involves real-time decision-making to ensure adherence to Good Manufacturing Practices (GMP) and requires shift work, including late afternoons and nights. **

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, and retirement savings plan

Skills & Requirements

Must-have

  • cGMP and GDP compliance knowledge
  • shift work availability including nights
  • on-site facility presence required
  • deviation investigation experience
  • CAPA and change control review

Nice-to-have

  • biotechnology plant startup experience
  • upstream or downstream process knowledge
  • strong organizational and communication skills
  • team player with independent work ability
  • proficiency in EBR/MES systems

Key Requirements

  • High school/GED plus 4 years QA experience OR Bachelor's degree plus 6 months experience
  • Must be willing to transition to second or third shift schedule
  • Experience in regulated pharmaceutical or biotechnology manufacturing environments

Work Rights

Not specified

Tailored Resume

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