Qa Operations Specialist

539

Dublin, Ireland
Gmp compliance
Quality operations support
Production documentation review
This role provides direct Quality support to the Upstream production area as part of a Quality IPT (Integrated Product Team)

Job Summary

  • This role provides direct Quality support to the Upstream production area as part of a Quality IPT (Integrated Product Team).
  • Responsible for review/approval of new and updated Master Batch Records / Electronic Batch Records and production documentation.
  • Participates as the quality member on cross functional projects and drives continuous improvement.

Matching Summary

This role provides direct Quality support to the Upstream production area as part of a Quality IPT (Integrated Product Team).

Skills & Requirements

Must-have

  • GMP Compliance
  • Quality Operations support
  • Production documentation review
  • Shop floor presence
  • Biotech industry experience

Nice-to-have

  • Continuous improvement initiatives
  • Cross-functional project participation
  • Problem-solving tools utilization
  • Strong interpersonal skills

Key Requirements

  • Minimum 5 years of relevant post-degree work experience
  • 2 years of working knowledge in biotech QA operations
  • Bachelor’s degree in scientific or engineering field (preferred)

Work Rights

Not specified

Tailored Resume

Cover Letter