This role involves developing and authoring protocols and reports for capital projects and revalidation aligned to approved testing plans
Job Summary
This role involves developing and authoring protocols and reports for capital projects and revalidation aligned to approved testing plans.
The position requires analyzing validation data to assess capability, identify trends, and recommend practical improvements while maintaining audit-ready documentation.
AstraZeneca offers an inclusive culture that champions diversity and collaboration, committed to lifelong learning and growth within a global science-led biopharmaceutical company.
Matching Summary
This role involves developing and authoring protocols and reports for capital projects and revalidation aligned to approved testing plans.
Skills & Requirements
Must-have
Develop IQ/OQ/PQ/PPQ protocols
Analyze validation and process data
Create risk assessments with controls
Review OCM and CAPA documentation
Coach teams on cGMP best practices
Nice-to-have
Understanding of sterilisation validation
Knowledge of computer system validation
Proficiency with Microsoft Office suite
Experience in continuous improvement
Strong collaborative communication skills
Key Requirements
2-year fixed-term contract
Experience in validation engineering
Strong attention to detail and analytical thinking