Validation Engineer

AstraZeneca

Cgmp
Product quality
Regulatory compliance
Develop and author protocols and reports (IQ/OQ/PQ/PPQ) for capital projects, revalidation, OCM, and CAPA, aligned to approved testing plans and schedules

Job Summary

  • Develop and author protocols and reports (IQ/OQ/PQ/PPQ) for capital projects, revalidation, OCM, and CAPA, aligned to approved testing plans and schedules.
  • Analyse validation and process data to assess capability, identify trends, and recommend practical improvements; create and maintain risk assessments with appropriate controls and mitigations.
  • At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit.

Matching Summary

Develop and author protocols and reports (IQ/OQ/PQ/PPQ) for capital projects, revalidation, OCM, and CAPA, aligned to approved testing plans and schedules.

Skills & Requirements

Must-have

  • cGMP
  • product quality
  • regulatory compliance
  • test protocol development
  • risk assessment
  • audit-ready documentation

Nice-to-have

  • continuous improvement
  • collaborative communicator
  • speak up
  • lifelong learning
  • entrepreneurial spirit

Key Requirements

  • Fixed-term role for 2 years
  • Strong attention to detail
  • Analytical thinking
  • Manage multiple priorities
  • Skilled problem solver

Work Rights

Not specified

Tailored Resume

Cover Letter