Qa Specialist – 12 Month Ftc

ADMF

College Park, Dublin, Ireland
Not specified (assumed on-site based on the nature of the role)
Experience in pharmaceutical or biotech industry
Strong understanding of gmp and quality systems
Ability to work in complex international matrix environment
ADMF is seeking a QA Specialist for a 12-month fixed-term contract at their Bulk Drug Substance facility in Dublin, Ireland. This role involves providing comprehensive quality oversight for manufacturing and testing processes, ensuring compliance with regulatory standards, and collaborating with various departments to maintain a robust Quality Management System

Job Summary

  • This role provides end-to-end quality oversight across manufacturing, testing, documentation, and product disposition at a Bulk Drug Substance facility.
  • The successful candidate will partner with Operations, QC, Engineering, Supply Chain, and QPs to maintain a robust Quality Management System.
  • You will play a pivotal role in safeguarding the quality of life-changing biologic medicines where your expertise directly protects patients.

Matching Summary

Match Score: 85

ADMF is seeking a QA Specialist for a 12-month fixed-term contract at their Bulk Drug Substance facility in Dublin, Ireland. This role involves providing comprehensive quality oversight for manufacturing and testing processes, ensuring compliance with regulatory standards, and collaborating with various departments to maintain a robust Quality Management System.

Skills & Requirements

Must-have

  • Experience in pharmaceutical or biotech industry
  • Strong understanding of GMP and quality systems
  • Ability to work in complex international matrix environment

Nice-to-have

  • Strong leadership presence and cross-functional influence
  • Fluency in written and spoken English
  • Experience with biologics operations

Key Requirements

  • Degree in Pharmacy, Biology, Biotechnology, Engineering, or relevant scientific discipline
  • Experience in pharmaceutical or biotech industry
  • Solid understanding of GMP and regulatory expectations

Work Rights

Not specified

Tailored Resume

Cover Letter