Document Control Administrator Ii- Spiddal Galway

813

Galway, Ireland
Good manufacturing practices (gmp)
Quality system guidelines
Electronic documentation systems
The primary purpose of this position is to support and perform documentation administration activities within the Quality function, adhering to Good Manufacturing Practices (GMP) and Quality system guidelines

Job Summary

  • The primary purpose of this position is to support and perform documentation administration activities within the Quality function, adhering to Good Manufacturing Practices (GMP) and Quality system guidelines.
  • Responsibilities include administrator support for change record implementation, control of document distribution and retrieval, and managing access to records and documents.
  • The role requires adherence to company policies, safety and quality requirements, and understanding of regulatory requirements such as FDA regulations and QMS.

Matching Summary

The primary purpose of this position is to support and perform documentation administration activities within the Quality function, adhering to Good Manufacturing Practices (GMP) and Quality system guidelines.

Skills & Requirements

Must-have

  • Good Manufacturing Practices (GMP)
  • Quality system guidelines
  • Electronic documentation systems
  • Quality Management Systems (QMS)
  • Good Documentation Practices (GDP)

Nice-to-have

  • Collaborative team environment
  • Focus on customer success
  • Continuous improvement mindset
  • Respectful interaction with others

Key Requirements

  • 2-3 years of experience
  • High school graduate or equivalent
  • Working knowledge of Electronic documentation systems
  • Understanding of Quality Management Systems

Work Rights

Not specified

Tailored Resume

Cover Letter