Validation Analyst

Thermo Fisher Scientific UK

Athlone, Ireland
Hybrid
Gmp documentation drafting and execution
Software development lifecycle support
Vendor installation management
Participates in project teams to guide system enhancements, review change requests, and ensure accurate testing and communication

Job Summary

  • Participates in project teams to guide system enhancements, review change requests, and ensure accurate testing and communication.
  • Provides validation support across the software development lifecycle, including drafting and executing GMP documentation.
  • Delivers ongoing user support and maintenance for validated systems.

Matching Summary

Participates in project teams to guide system enhancements, review change requests, and ensure accurate testing and communication.

Skills & Requirements

Must-have

  • GMP documentation drafting and execution
  • Software development lifecycle support
  • Vendor installation management
  • User support for validated systems
  • Troubleshooting software defects

Nice-to-have

  • Client-focused approach
  • Positive attitude and enthusiasm
  • Adaptability to changing priorities

Key Requirements

  • Bachelor's degree required
  • 2-5 years GMP experience
  • Experience with standalone hardware and software systems
  • Proficiency in Microsoft Office Suite
  • Understanding of SDLC and clinical trials processes

Work Rights

Not specified

Tailored Resume

Cover Letter