Investigation Process Owner

Thermo Fisher Scientific UK

Monza, Italy
Gmp regulations knowledge
Batch record review
Deviation investigations
Join Thermo Fisher Scientific and discover meaningful work that makes a positive impact on a global scale

Job Summary

  • Join Thermo Fisher Scientific and discover meaningful work that makes a positive impact on a global scale.
  • As a Lead QA Technician, you will contribute to ensuring product quality and regulatory compliance in pharmaceutical manufacturing operations.
  • Your expertise will help maintain high standards of quality while supporting the production of life-changing medicines.

Matching Summary

Join Thermo Fisher Scientific and discover meaningful work that makes a positive impact on a global scale.

Skills & Requirements

Must-have

  • GMP regulations knowledge
  • batch record review
  • deviation investigations
  • CAPA management
  • aseptic manufacturing processes
  • quality documentation systems

Nice-to-have

  • cross-functional team collaboration
  • clean room operations
  • guide and develop team members

Key Requirements

  • 4 years pharmaceutical quality assurance experience
  • Chemistry, Pharmacy, Biology, Biotechnology degree preferred
  • Advanced proficiency in quality documentation systems
  • Experience supporting regulatory inspections
  • Experience with clean room operations and gowning procedures preferred

Work Rights

Not specified

Tailored Resume

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