Qa Specialist

Trzdev15

College Park, Dublin
Cgmp oversight for manufacturing activities
Review and approve batch records
Support inspection readiness
You’ll provide end-to-end quality oversight across manufacturing, testing, documentation, and product disposition

Job Summary

  • You’ll provide end-to-end quality oversight across manufacturing, testing, documentation, and product disposition.
  • This is a high-impact role at the heart of our biologics operation, ensuring every batch we produce is safe and compliant.
  • Your expertise directly protects patients and strengthens a world-class manufacturing site.

Matching Summary

You’ll provide end-to-end quality oversight across manufacturing, testing, documentation, and product disposition.

Skills & Requirements

Must-have

  • cGMP oversight for manufacturing activities
  • review and approve batch records
  • support inspection readiness

Nice-to-have

  • strong communication and presentation skills
  • ability to work in international matrix environment
  • strong leadership presence

Key Requirements

  • experience in pharmaceutical or biotech industry
  • degree in Pharmacy, Biology, or relevant discipline

Work Rights

Not specified

Tailored Resume

Cover Letter