Qa Specialist – 12 Month Ftc

AstraZeneca

College Park, Dublin
Cgmp oversight for manufacturing
Review and approve batch records
Quality risk assessments
Provide end-to-end quality oversight across manufacturing, testing, documentation, and product disposition

Job Summary

  • Provide end-to-end quality oversight across manufacturing, testing, documentation, and product disposition.
  • You’ll be a key partner to Operations, QC, Engineering, Supply Chain and QPs, helping maintain a robust Quality Management System and supporting inspection readiness across the site.
  • Play a pivotal role in safeguarding the quality of life-changing biologic medicines, where your expertise directly protects patients and strengthens a world-class manufacturing site.

Matching Summary

Provide end-to-end quality oversight across manufacturing, testing, documentation, and product disposition.

Skills & Requirements

Must-have

  • cGMP oversight for manufacturing
  • Review and approve batch records
  • Quality risk assessments
  • Inspection readiness support
  • QMS elements oversight

Nice-to-have

  • Thrive in fast-paced environment
  • Meaningful difference maker
  • International matrix environment

Key Requirements

  • Degree in Pharmacy, Biology, Biotechnology, Engineering, or scientific discipline
  • Experience in pharmaceutical or biotech industry
  • Fluency in written and spoken English

Work Rights

Not specified

Tailored Resume

Cover Letter