Biopharmaceutical Validation Expert

19 hours ago


Oxford, Oxfordshire, United Kingdom Oxford Biomedica Full time
Job Description

We are seeking a highly skilled Biopharmaceutical Validation Expert to join our team at Oxford Biomedica. In this role, you will be responsible for preparing and executing validation protocols and reports for Process Validation/Process Performance Qualification (PPQ). You will also own quality records on behalf of the Validation Department and support validation activities during Technology Transfer.

About the Role

This is an exciting opportunity to contribute to the maintenance of overall department KPIs relating to validation of equipment, facilities, utilities, processes, and computerised systems. You will work closely with the Validation Department to ensure that all manufacturing processes meet GMP regulations and industry guidelines.

Key Responsibilities
  • Preparation and execution of validation protocols and reports
  • Owning quality records on behalf of the Validation Department
  • Supporting validation activities during Technology Transfer
Requirements
  • A Degree in a Science or Engineering discipline
  • Working knowledge of current standards, GMP regulations, and industry guidelines
  • Demonstrable experience of validation of manufacturing processes in a biopharmaceutical industry
  • Experience of working within a GMP Quality Management System


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