Associate Quality Control Analytical

AstraZeneca

Rockville, MD, US
Base: $55,920.80 - $83,881.20; bonus/equity: short...
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Cgmp lot release testing experience
Elisa pcr flow cytometry skills
Alcoa+ data integrity compliance
** AstraZeneca is seeking an Associate Quality Control Analytical in Rockville, MD, to support cGMP lot release and stability testing for cell therapy products. The ideal candidate should have an associate's degree and relevant lab experience, focusing on quality execution and compliance with established procedures. **

Job Summary

  • The role supports cGMP lot release and stability testing for cell therapy products while maintaining high quality and data integrity.
  • Candidates must complete assays such as automated cell counting, ELISA, and PCR following approved methods and regulatory expectations.
  • The position offers eligibility for short-term incentive bonuses, equity-based awards, and comprehensive health and retirement benefits.

Matching Summary

Match Score: 75

** AstraZeneca is seeking an Associate Quality Control Analytical in Rockville, MD, to support cGMP lot release and stability testing for cell therapy products. The ideal candidate should have an associate's degree and relevant lab experience, focusing on quality execution and compliance with established procedures. **

Salary

Base: $55,920.80 - $83,881.20; Bonus/Equity: Short-term incentives and equity-based awards available; Benefits: Qualified retirement programs, paid time off, health, dental, and vision coverage

Skills & Requirements

Must-have

  • cGMP lot release testing experience
  • ELISA PCR flow cytometry skills
  • ALCOA+ data integrity compliance
  • SOP adherence and documentation
  • Cell culture handling techniques

Nice-to-have

  • Enthusiasm to develop new technical skills
  • Positive solutions-oriented attitude
  • Willingness to support weekend testing
  • Cross-functional collaboration skills
  • Flexibility in evolving environment

Key Requirements

  • Associate's degree with 3 years lab experience
  • Experience in pharmaceutical or biotech settings
  • Understanding of core cGMP concepts

Work Rights

Not specified

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